Compositions Useful for the Treatment of Diabetes and Other Chronic Disorder

ABSTRACT

The present invention provides a supramolecular protein assembly useful as a protein therapeutics for the treatment of metabolic disorders particularly diabetes. The supramolecular protein assembly disclosed in the present invention consists of insoluble and aggregated oligomers the protein. The invention also provides pharmaceutical compositions comprising supramolecular protein assembly. The composition disclosed in the present invention particularly comprises supramolecular insulin assembly.

TECHNICAL FIELD

The present invention relates to protein therapeutics for treatment of diabetes and other chronic diseases:

BACKGROUND OF INVENTION

Protein medications are the most rapidly expanding class of therapeutics, serving patients with diabetes, cancer, cardiovascular, renal, gastrointestinal, rheumatologic and neurological diseases among many others. The therapeutic and commercial value of protein as therapeutics including insulin, erythropoietin, G-CSF, plasminogen activator, and interferons is undisputed. Improved proteins or their formulations have enhanced the therapeutic efficacy of these parent products, by increasing their potency, time of action, and other properties.

Diabetes is a chronic disease characterized by either the inability of the body to produce insulin (Type 1) or the failure to respond to it (Type II) (http://www.who.int/diabetes/en, King, H., Aubert, R. E. & Herman, W. H. Global burden of diabetes, 1995-2025: Prevalence, numerical estimates, and projections. Diabetes Care 21, 1414-1431 (1998)). There is an emerging global epidemic of diabetes of both Type I and Type II forms. Nearly 1.1 million diabetics succumbed to death in 2005 (Dunstan, D. W., Zimmet, P. Z., Welborn, T. A., De Courten, M. P., Cameron, A. J., et al. The rising prevalence of diabetes and impaired glucose tolerance: The Australian Diabetes, Obesity and Lifestyle Study. Diabetes Care 25, 829-834 (2002)). Its economic consequences are even more staggering as people may live for years with diabetes, their cause of death is often recorded as heart diseases and kidney failures, both arising as a secondary consequence of diabetes.

Restoring the normal metabolic milieu by administration of insulin from outside and thereby minimizing the risk of secondary complications has become an essential feature of diabetic treatment. The current therapy involves multiple daily subcutaneous (SC)/intramuscular (IM) injections of insulin, which leads to a heavy burden of compliance on patients. This in turn has led to alternative, less invasive routes of delivery. Attempts to exploit the nasal, oral, gastrointestinal and transdermal routes, till date have been mostly unsuccessful. Although a conventional insulin regimen for type I diabetes with twice-daily insulin injections is effective in controlling postprandial blood glucose levels, this treatment is of limited value due to its failure to control fasting hyperglycemia (Cardona, K., Korbutt, G. S., Milas, Z., Lyon, J., Cano, J., Jiang, W., Bello-Laborn, H., Hacquoil B, Strobert E, Gangappa S, Weber C J, Pearson T C, Rajotte R V, Larsen C P. Long-term survival of neonatal porcine islets in nonhuman primates by targeting costimulation pathways. Nat Med. March; 12(3), 304-6 (2006)). Patients with diabetes mellitus need insulin therapy to boost intrinsic insulin supply once or twice a day. Also, post-prandial glucose homeostasis is maintained through regular insulin injections before each meal. Intensive insulin therapy delays the onset and or slows the progression of secondary complications, yet patients remain at a high risk of fasting hypoglycemia. An insulin formulation which releases insulin in a controlled manner for long periods of time would free the patients from the need to administer multiple doses of insulin daily. The present invention provides a composition for a prolonged release of insulin for treating diabetes, both type I and II.

SUMMARY OF THE INVENTION

The present invention discloses protein therapeutics for treatment of diabetes and other chronic diseases. The present invention particularly discloses supramolecular protein assembly, wherein the supramolecular protein assembly comprises the insoluble and aggregated oligomeric form of the protein for example insulin, glucagon, calcitonin, a peptide GNNQQNY, transthyretin (TTR), human growth hormone, blood clotting factors, albumin, human follicle stimulating hormone (FSH), human chorionic gonadotropin (HCG), Interleukin-1 Receptor Antagonist (IL-1RA), extendin-4 and erythropoietin. The present invention also discloses the pharmaceutical composition comprising supramolecular protein assembly.

The supramolecular protein assembly and compositions disclosed in the present invention are useful for the treatment of metabolic disorders particularly diabetes, and other chronic and inflammatory diseases such as rheumatoid arthritis, osteoporosis, chronic inflammatory and peripheral pain, sepsis, and allergy where a continuous and prolonged therapy is required using peptides, proteins or small drug molecules.

One aspect of the present invention provides a supramolecular protein or peptide assembly (SPA) useful as protein therapeutics for the treatment of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus and complications thereof; or chronic diseases selected from the group consisting of osteoporosis, arthritis, cancer, endotoxic shock, wherein the assembly comprises insoluble and aggregated oligomeric form of the protein or peptide.

Another aspect of the present invention provides a supramolecular insulin assembly (SIA) useful as protein therapeutics for the treatment of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus and complications thereof, wherein the assembly comprises insoluble and aggregated oligomeric form of insulin.

Another aspect of the present invention provides a supramolecular calcitonin assembly (SCA) useful as protein therapeutics for the treatment of osteoporosis, wherein the assembly comprises insoluble and aggregated oligomeric form of calcitonin.

Another aspect of the present invention provides a supramolecular ibuprofen assembly (SIbA) useful as protein therapeutics for the treatment of arthritis, wherein the assembly comprises insoluble and aggregated form of peptide tagged ibuprofen.

Yet another aspect of the present invention provides a supramolecular extendin-4 assembly (SEA) useful as protein therapeutics for the treatment of diabetes, wherein the assembly comprises insoluble and aggregated oligomeric form of extendin-4.

Further the present invention provides a pharmaceutical composition useful as protein therapeutics for the treatment of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus and complications thereof or chronic diseases selected from a group consisting of osteoporosis, arthritis, cancer, endotoxic shock, wherein the composition comprising therapeutically effective amount of the supramolecular protein or peptide (SPA) assembly disclosed in the present invention.

The present invention also provides a pharmaceutical composition for the treatment of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus and complications thereof, the composition comprising therapeutically effective amount of the supramolecular insulin assembly (SIA).

The present invention also provides a pharmaceutical composition for the treatment of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus and complications thereof, the composition comprising therapeutically effective amount of the supramolecular insulin assembly (SIA) and supramolecular extendin-4 assembly (SEA) of the present invention.

In another aspect, the present invention provides a pharmaceutical composition for the treatment of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus and complications thereof, the composition comprising therapeutically effective amount of the supramolecular insulin assembly (SIA) and supramolecular extendin-4 assembly (SEA) of the present invention.

In another aspect of the present invention a pharmaceutical composition is provided for the treatment of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus and complications thereof, the composition comprising therapeutically effective amount of the supramolecular insulin assembly (SIA) and supramolecular extendin-4 assembly (SEA) disclosed in the present invention.

Also provided is a pharmaceutical composition for the treatment of osteoporosis, the composition comprising supramolecular calcitonin assembly (SCA) of the present invention.

In yet another invention a pharmaceutical composition for the treatment of arthritis and arthritic pain, the composition comprising supramolecular ibuprofen assembly (SIbA) disclosed in the present invention.

Further aspect of the present invention is to provide a process of preparation of supramolecular insulin assembly (SIA) disclosed in the present invention, the process comprising; dissolving insulin at a temperature of about 25 to 60° C. in a solution having pH in the range of 1.5 to 7.8; and incubating the above for a period of 6-48 hours with constant stirring to obtain Supramolecular Insulin Assembly (SIA), wherein SIA comprises insoluble and aggregated oligomeric form of insulin.

Yet another invention is to provide a process of preparation of supramolecular calcitonin assembly (SCA) disclosed in the present invention, the process comprising dissolving calcitonin at a temperature of about 25 to 60° C. in a solution having pH in the range of about 4.0 to 8.0; and incubating the above for a period of 6-48 hours with constant stirring to obtain Supramolecular Calcitonin Assembly (SCA), wherein SCA comprises insoluble and aggregated oligomeric form of calcitonin

A process of preparation of supramolecular ibuprofen-tagged peptide assembly (SIbA) is also disclosed in the present invention, the process comprising dissolving ibuprofen-peptide at a temperature of about 25 to 60° C. in a solution having pH in the range of about 3.5 to 7.6; and incubating the above for a period of 6-48 hours with constant stirring to obtain Supramolecular Ibuprofen Assembly (SIbA), wherein SIbA comprises insoluble and aggregated oligomeric form of peptide tagged ibuprofen.

The present invention also provides a process of preparation of supramolecular Extendin assembly as disclosed in the present invention, the process comprising dissolving extendin 4 at a temperature of about 25 to 60° C. in a solution having pH in the range of about 2.0 to 7.6; and incubating the above for a period of 6-192 hours with constant stirring to obtain Supramolecular Extendin Assembly (SEA), wherein SEA comprises insoluble and aggregated oligomeric form of Extendin-4.

Further, the present invention provides a method for treating of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus or chronic diseases selected from a group consisting of osteoporosis, arthritis, cancer, endotoxic shock, wherein the method comprising administering to a subject in need thereof a therapeutically effective amount of the pharmaceutical composition which is effective for the alleviation of the disorder or disease.

The present invention also provides a method for treating of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus, wherein the method comprising administering to a subject in need thereof a therapeutically effective amount of the pharmaceutical composition comprising the supramolecular insulin assembly.

One of the aspect of the present invention is to provide a method for treating osteoporosis, wherein the method comprising administering to a subject in need thereof of a therapeutically effective amount of the pharmaceutical composition comprising the supramolecular calcitonin assembly for treating osteoporosis.

Another aspect of the present invention provides a method for treating arthritic pain, wherein the method comprising administering to a subject in need thereof a therapeutically effective amount of the pharmaceutical composition comprising supramolecular ibuprofen assembly which is effective for the alleviation of the disease.

Yet another aspect of the present invention provides use of a supramolecular protein assembly for the treatment of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus or chronic diseases selected from a group consisting of osteoporosis, arthritis, cancer and endotoxic shock.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows kinetics of fibril formation at pH 2.0 and 7.0 monitored with 50 μM Th-T fluorescence of recombinant human (rH) and bovine insulin.

FIG. 2

-   -   (a) Shows in-vitro release of insulin from supramolecular         insulin assembly II (also referred to as pre-amyloid insulin II         intermediate) of bovine and rH insulin monitored by absorbance         at 280 nm and intrinsic tyrosine fluorescence. The Th-T         intensity of solution inside the dialysis membrane at 0 h and 15         days is also given.     -   (b) shows in vitro monomer release kinetics from the various         supramolecular insulin assembly intermediates of bovine insulin.     -   (c) shows in vitro monomer release kinetics from the various         supramolecular insulin assembly intermediates of rH-insulin.     -   (d) shows in vitro release kinetics of SIA II (alternatively         preamyloid) formed at pH 7.0 monitored under constant 1 ml PBS         solution.

FIG. 3 shows Congo-Red binding studies with native insulin, supramolecular insulin assembly II (alternatively pre-amyloid insulin II), supramolecular insulin assembly III (alternatively pre-amyloid insulin III) and insulin amyloid (bovine and human).

FIG. 4 shows fourier transform infrared (FTIR) spectroscopic characterization of r-human and bovine insulin.

FIG. 5 shows morphologies of supramolecular insulin assembly (alternatively pre-amyloid insulin) intermediates and insulin fibrils studied by Atomic Force Microscopy (AFM):

-   -   (a) insulin monomer     -   (b) supramolecular insulin assembly I (alternatively pre-amyloid         insulin I) intermediate, pH 7.0 of Bovine insulin,     -   (c) supramolecular insulin assembly II (alternatively         pre-amyloid insulin II), pH 7.0 of Bovine insulin,     -   (d) supramolecular insulin assembly intermediate III         (alternatively pre-amyloid insulin III), pH 7.0 of Bovine         insulin,     -   (e) supramolecular insulin assembly-I, pH 7.0 of rH-insulin,     -   (f) supramolecular insulin assembly-II, pH 7.0 of rH-insulin,     -   (g) supramolecular insulin assembly-III, pH 7.0 of rH-insulin,     -   (h) fully formed fibrils at pH 7.0, (i) shows supramolecular         insulin assembly (alternatively pre-amyloid insulin)         intermediate formed at 6 hrs, pH 2.0 at 37° C.,     -   (j) amyloid fibril formed at pH 2.0,

FIG. 6 shows negative staining TEM micrographs of insulin fibrils and the intermediates during the formation of supramolecular insulin assembly

-   -   (a) Supramolecular insulin assembly I (alternatively pre-amyloid         insulin I), pH 7.0,     -   (b) Supramolecular insulin assembly II (alternatively         pre-amyloid insulin II), pH 7.0,     -   (c) Supramolecular insulin assembly III (alternatively         pre-amyloid insulin III), pH 7.0,     -   (d) Mature fibers at pH 7.0,     -   (e) Fiber formed at pH 2.0, 37° C.

FIG. 7 shows in vivo efficacy of supramolecular insulin assembly (alternatively pre-amyloid insulin) in glucose homeostasis.

-   -   (a) Blood glucose level in response to various dosages of         supramolecular insulin assembly-II (bovine) administered both         subcutaneously and intramuscularly.     -   (b) Blood glucose level in response to various dosages of         supramolecular insulin assembly-II (r-human) administered both         subcutaneously and intramuscularly.

FIG. 8 shows Post-prandial blood glucose levels monitored over a period of 135 days after administration of bovine SIA-II

-   -   (a) Bovine insulin     -   (b) rH insulin.

FIG. 9 shows Pre-prandial blood glucose levels monitored over a period of 160 days after administration of human SIA-II

-   -   (a) Bovine insulin     -   (b) rH insulin.

FIG. 10 shows blood glucose level monitored after administration of insulin amyloid formed at pH 2.0 and 7.0.

FIG. 11 shows body weight profile of SIA-II treated diabetic rats, diabetic control and non-diabetic control rats.

FIG. 12 shows blood glucose profile during intraperitoneal glucose tolerance test (IPGTT)

FIG. 13 shows

-   -   (a) quantification of serum rH and bovine insulin released from         corresponding SIA-II using solid state ELISA in STZ treated rats         in response to supramolecular insulin assembly (alternatively         pre-amyloid insulin) injected SC or IM.     -   (b) Quantification of serum bovine insulin during IPGTT         experiment.     -   (c) Serum rat insulin ELISA performed for IPGTT to determine the         endogenous level of insulin in response to infused glucose.

FIG. 14 shows ¹²⁵I labeled insulin SIA II treatment of STZ diabetic rats

-   -   (a) CPM/ml profile in serum of animals treated with 100 μg of         labeled supramolecular insulin assembly up to 25 days. The         profile for 24 h is given in inset     -   (b) Blood glucose (mg/dL) and bovine insulin (ng/ml) released in         vivo profile for 36 days. The profile for 24 h is shown in inset

FIG. 15 shows Tricine-SDS-PAGE of serum from animals treated with labeled SIA II. Coommassie stoning (left) and phosphor images (rest after left) of serum of 1-28 days after treatment either subcutaneously (upper panel) or intramuscularly (middle panel). The lower panel shows in vitro released monomers from SIA II.

FIG. 16 shows hyperglycemic clamp studies after treatment with supramolecular insulin assembly II. GIR-glucose infusion rate (mg/kg/min)

FIG. 17 shows Western blot (WB) analysis of cultured adipocytes for insulin signaling cascade Adipocytes treated with (a) PBS, insulin, SIA-II, insulin released from SIA-II, (b) serum as indicated, and analysed for insulin signaling.

FIG. 18 shows male Wistar rats rendered diabetic with STZ and treated subcutaneously with supramolecular insulin assembly II (alternatively pre-amyloid insulin II) and checked for the presence of residual supramolecular insulin assembly using Congo red and the occurrence of inflammation respectively.

-   -   (a) Subcutaneous Congo red stained sections (i-v), Congo red         Birefringence (vi-x), H & E stained sections (xi-xv), and         Immunostained section (xvi-xx) from week 1 to week 12.     -   (b) Intramuscularsections stained with Congo red (i-v), Congo         red Birefringence (vi-x) H & E stained sections (xi-xv), and         Immunostained section (xvi-xx) from week 1 to week 12.

FIG. 19 shows

-   -   (a) LPS from E. coli was injected to subcutaneous and muscle         tissues as a positive control for infiltration of inflammatory         cells. Immunostained SC (i) and IM (ii) section, and H&E stained         SC (iii) and IM (iv) section.     -   (b) Insulin amyloid fibers formed at pH 2.0 injected SC were         monitored for 1, 4, 8 and 12 weeks using Congo red stained         sections (i-iv) and Congo Red Birefringence (v-viii).

FIG. 20 shows blood glucose profile of rH-insulin SIA-II treatment of rats rendered diabetic using Alloxan.

-   -   (a) Fasting     -   (b) Non-fasting Blood     -   (c) Human Insulin quantification in serum using solid state         ELISA as per the manufacturer's protocol.

FIG. 21 shows monitoring cataract formation in

-   -   (a) STZ-treated Rat.     -   (b) Control Rat.     -   (c) Insulin-treated Rats.     -   (d) Supramolecular insulin assembly treated Rats.

FIG. 22 shows heart, kidney and liver tissue were sectioned and examined for amyloid deposition by staining with CR. Cellular morphology was also assessed using H&E Staining.Congo red Birefringence of heart kidney and liver (i-iii), Congo red stained sections (iv-vi), H&E staining of heart, kidney and liver (vii-ix).

FIG. 23 shows detection of Rat Insulin degrading enzyme (IDE) after treatment with SIA-II.

FIG. 24 shows screening for anti-insulin antibody in Rat serum treated with SIA-II.

FIG. 25 shows MTT assay for cell proliferation: MCF 7 cells were assayed for their growth kinetics by the administration of PBS, pH 7.4, human/bovine insulin (20 nM), SIA II (Human/bovine insulin), released insulin monomers from SIA II (20 nM), Insulin like Growth Factor I (IGF-1) (6 ng/ml).

FIG. 26 shows blood glucose level in response to various dosages of supramolecular insulin assembly administered both subcutaneously and intramuscularly in mice rendered diabetic using STZ. Human SIA-II injected (a) subcutaneously, (b) intramuscularly and (c) bovine SIA-II subcutaneously at indicated dosage.

FIG. 27 shows blood glucose level in response to supramolecular insulin assembly administered subcutaneously in rabbit rendered diabetic using STZ.

FIG. 28 shows blood glucose profile of Type II diabetic rats given various treatment as indicated in the figure, over a period of 35 days.

FIG. 29 shows kinetics of calcitonin fibril formation in PBS at 37° C. under stagnant condition. Fibril formation was monitored by turbidity measurement at 400 nm.

FIG. 30 shows in vitro release profile of calcitonin released from SCA-II under constant volume of 1 ml and dialyzing against membrane in 2% mannitol (5 ml). The release was observed by monitoring absorbance at 275 nm.

FIG. 31 shows profile of calcitonin released from SCA-II in the serum of ovariectomized rat of different treatment group. Calcitonin in serum was measured by an immunoassay kit.

FIG. 32 shows

-   -   (a) Hot plate test for arthritic pain. Arthritis was induced in         male Wistar rats using Kaolin/carrageenin. After half and hour,         the rats were given respective drug dosages as indicated in the         figure. Rats were placed on the analgesiometer at 55° C., one         hour after treatment. The latency in licking their paw was         determined with the help of a stop watch. Results are expressed         as mean±S.E.M (n=5) of three independent experiments done on the         same day.     -   (b) Hot plate test for evaluating arthritic pain. Arthritis was         induced in male Wistar rats using Kaolin/carrageenin. After 30         min, the rats were given respective drug dosages as indicated in         the figure. Ibuprofen was administered daily orally, and after         an hour placed on the anagesiometer at 55° C. Results are         expressed as mean±S.E.M (n=5) of three independent experiments         done on the same day.

FIG. 33 shows the inhibition of carrageenin-induced rat paw oedema by treatment with supramolecular Ibuprofen-TTR assembly. The oedema is expressed as the increase in volume (m1) of the injected paw compared to its basal volume. Results are expressed as mean±S.E.M (n=5) of three independent experiments done on the same day

DETAILED DESCRIPTION OF THE INVENTION

The present invention provides protein therapeutics for treatment of diabetes and other chronic diseases/disorders. The present invention particularly provides supramolecular protein or peptide (SPA) assembly, wherein the supramolecular protein or peptide assembly (SPA) comprises the insoluble and aggregated oligomeric form of the protein, wherein the protein is selected from a group consisting of insulin, glucagon, calcitonin, GNNQQNY, transthyretin (TTR), human growth hormone, blood clotting factors, albumin, human follicle stimulating hormone (FSH), human chorionic gonadotropin (HCG), Interleukin-1 Receptor Antagonist (IL-1RA), extendin-4 and erythropoietin. The present invention also provides the pharmaceutical compositions comprising supramolecular protein assembly.

The supramolecular protein or peptide (SPA) assembly and pharmaceutical compositions disclosed in the present invention are useful for the treatment of metabolic disorders particularly diabetes and other chronic and inflammatory diseases such as rheumatoid arthritis, osteoporosis, chronic inflammatory and peripheral pain, sepsis, and allergy where a continuous and prolonged therapy is required using peptides, proteins or small drug molecules.

The present invention also provides the feasibility of treating Type II diabetes and a number of chronic ailments such as arthritic pain as well as acute symptoms eg: trauma induced pain. In case of arthritic pain, drug molecules tagged to peptides such as GNNQQNY, which forms a stable oligomer, will result in a slow and sustained release of the anti arthritic drug for relieving pain in such subjects. The methodology of the present invention can also be extended for the treatment of osteoporosis using calcitonin, a peptide hormone for therapy.

The term “supramolecular protein assembly” also refers to an intermediate form of a protein formed during the process of fibirilization and is characterized by an oligomeric association of peptide/protein monomers.

The term “supramolecular insulin assembly” or “SIA” used herein refers to supramolecular insulin assembly I, II and III, which are the insoluble and aggregated oligomeric form of insulin.

The term “SIA I” used herein refers to “supramolecular insulin assembly” at stage I, wherein “SIA I” comprises the insoluble and aggregated oligomeric form of insulin, wherein the oligomers consists of elongated clusters having pearl like arrangement of insulin monomer.

The term “SIA II” used herein refers to “supramolecular insulin assembly” at stage II, wherein “SIA II” comprises the insoluble and aggregated oligomeric form of insulin, wherein the oligomers of insulin are arranged in linear association of elongated clusters having pearl like arrangement of insulin monomer.

The term “SIA III” used herein refers to “supramolecular insulin assembly” at stage III, wherein “SIA III” consists of a dense, linear association of oligomeric form of insulin.

SIA at stage III i.e. SIA II consist of about 90% of SIA-II.

The term “supramolecular Ibuprofen assembly” or “SIbA” used herein refers to supramolecular Ibuprofen assembly, which are the insoluble and aggregated form of peptides GNNQQNY, NFLVH, DFNKF, NFGAIL and KFFE covalently linked (tagged) with a pain killer Ibuprofen.

The term “supramolecular calcitonin assembly” or “SCA” used herein refers to supramolecular calcitonin assembly, which is the insoluble and aggregated oligomeric form of calcitonin.

In accordance with the present invention, one embodiment provides a supramolecular protein or peptide assembly (SPA) useful as protein therapeutics for the treatment of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus and complications thereof; or chronic diseases selected from the group consisting of osteoporosis, arthritis, cancer, endotoxic shock, wherein the assembly comprises insoluble and aggregated oligomeric form of said protein or peptide.

Another embodiment of the present invention provides the protein or a peptide for preparation of supramolecular protein assembly disclosed in the present invention, wherein the protein is selected from the group consisting of insulin, glucagon, calcitonin, transthyretin (TTR), human growth hormone, blood clotting factors, albumin, human follicle stimulating hormone (FSH), human chorionic gonadotropin (HCG), Interleukin-1 Receptor Antagonist (IL-1RA), extendin-4 and erythropoietin or the peptide GNNQQNY is used.

In another embodiment, the present invention provides a supramolecular insulin assembly (SIA) useful as protein therapeutics for the treatment of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus and complications thereof, wherein the assembly comprises insoluble and aggregated oligomeric form of insulin.

In yet another embodiment, the present invention provides the supramolecular insulin assembly (SIA) comprising insoluble and aggregated oligomeric form of insulin as SIA I, SIA II, SIA III stages or combination thereof, wherein SIA I consists of elongated clusters having pearl like arrangement of insulin monomer, SIA II consists of linear association of elongated clusters having pearl like arrangement of insulin monomer and SIA III consists of about 90% SIA-II, that is a dense, linear association of insulin oligomers.

In further embodiment, there is provided the supramolecular insulin assembly (SIA) as disclosed in the present invention, wherein the assembly comprises insoluble and aggregated oligomeric form of insulin at SIA II stage, wherein SIA II stage consists of linear association of elongated clusters having pearl like arrangement of insulin monomer.

In additional embodiment, there is provided the supramolecular insulin assembly (SIA) as disclosed in the present invention, wherein the assembly shows sharp peak at 1647-1645 cm⁻¹ in Fourier Transform infrared spectroscopy (FTIR).

In one embodiment, the present invention provides the supramolecular insulin assembly (SIA), wherein the insulin is recombinant Human insulin.

In another embodiment, the present invention provides the supramolecular insulin assembly (SIA), wherein the insulin is human, bovine or pig insulin.

One embodiment of the present invention provides the supramolecular insulin assembly (SIA), wherein the assembly releases insulin monomers at a rate ranging from about 0.2 to 0.6 IU per hour in vitro.

Another embodiment of the present invention provides the supramolecular insulin assembly (SIA), wherein rate of release of insulin is in a range of 0.1 to 5.4 ng/ml for about 7 to 180 days.

Yet another embodiment of the present invention provides the supramolecular insulin assembly (SIA), wherein rate of release of insulin is in a range of 0.5-1.5 ng/ml for at up to 180 days.

Further embodiment of the present invention provides the supramolecular insulin assembly (SIA), wherein the assembly upon administration maintains near-normoglycemic level (120±30 mg/dl) for at up to 180 days in a subject in need thereof.

In one embodiment of the present invention, there is provided the supramolecular insulin assembly (SIA), wherein a single dose of the assembly upon administration maintains near-normoglycemic level (120±30 mg/dl) for from 4-180 days in a subject in need thereof, wherein concentration of the assembly in the dose is in the range of 25 to 750 μg.

In another embodiment of the present invention, there is provided the supramolecular insulin assembly (SIA), wherein a single dose of the assembly upon administration maintains near-normoglycemic level (120±30 mg/dl) for at least up to 180 days in a subject in need thereof, wherein concentration of the assembly in the dose is in the range of 150 to 250 μg.

In yet another embodiment of the present invention there is provided the supramolecular insulin assembly (SIA), wherein the assembly upon administration releases insulin monomers.

The present invention also provides a supramolecular calcitonin assembly (SCA) useful as protein therapeutics for the treatment of osteoporosis, wherein said assembly comprises insoluble and aggregated oligomeric form of calcitonin.

The supramolecular calcitonin assembly (SCA) disclosed in the present invention upon administration releases calcitonin for about 55-60 days in a subject in need thereof.

Further the present invention provides the supramolecular protein assembly, wherein the peptide in assembly is coupled with a small molecule drug.

The present invention also provides a supramolecular ibuprofen assembly (SIbA) useful as protein therapeutics for the treatment of arthritis, wherein the assembly comprises insoluble and aggregated form of peptide tagged ibuprofen.

One embodiment of the present invention relates to the supramolecular ibuprofen assembly (SIbA) tagged with peptide, wherein the peptide is selected from the group consisting of GNNQQNY, NFGAIL, NFLVH, DFNKF and KFFE.

The present invention also provides a supramolecular extendin-4 assembly (SEA) useful as protein therapeutics for the treatment of diabetes, wherein the assembly comprises insoluble and aggregated oligomeric form of extendin-4.

One embodiment of the present invention provides the supramolecular protein assembly disclosed in the present invention acts as a prodrug,

Another embodiment of the present invention provides the supramolecular protein assembly disclosed in the present invention acts as a prodrug, wherein the assembly is selected from a group consisting of supramolecular insulin assembly (SIA), supramolecular calcitonin assembly (SCA), supramolecular ibuprofen assembly (SIbA) and supramolecular extendine-4 assembly (SEA).

In one embodiment of the present invention, there is provided the supramolecular protein assembly which is non cytotoxic.

In another embodiment of the present invention, there is provided the supramolecular protein assembly which is non cytotoxic, wherein the assembly is selected from a group consisting of supramolecular insulin assembly (SIA), supramolecular calcitonin assembly (SCA), supramolecular ibuprofen assembly (SIbA) and supramolecular extendine-4 assembly (SEA).

In accordance with the present invention, one embodiment provides a pharmaceutical composition useful as protein therapeutics for the treatment of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus and complications thereof or chronic diseases selected from a group consisting of osteoporosis, arthritis, cancer, endotoxic shock, wherein the composition comprising therapeutically effective amount of the supramolecular protein or peptide (SPA) assembly as disclosed in the present invention.

One embodiment relates to the pharmaceutical composition comprising the supramolecular protein or peptide (SPA) assembly of the present invention, wherein the protein or a peptide is selected from the group consisting of insulin, glucagon, calcitonin, transthyretin (TTR), human growth hormone, blood clotting factors, albumin, human follicle stimulating hormone (FSH), human chorionic gonadotropin (HCG), IL-1RA, extendin-4, erythropoietin GNNQQNY and other peptides.

The present invention further provides a pharmaceutical composition for the treatment of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus and complications thereof, the composition comprising therapeutically effective amount of the supramolecular insulin assembly (SIA) of the present invention.

In addition, in one embodiment the present invention provides a pharmaceutical composition for the treatment of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus and complications thereof, said composition comprising therapeutically effective amount of the supramolecular insulin assembly (SIA), wherein the assembly comprises insoluble and aggregated oligomeric form of insulin as SIA I, SIA II, SIA III stages or combination thereof, wherein SIA I consists of elongated clusters having pearl like arrangement of insulin monomer, SIA II consists of linear association of elongated clusters having pearl like arrangement of insulin monomer and SIA III consists of about 90% SIA-II, that is a dense, linear association of insulin oligomers.

In another embodiment, the present invention provides the supramolecular insulin assembly (SIA), wherein the assembly comprises insoluble and aggregated oligomeric form of insulin at SIA II, wherein SIA II consists of linear association of elongated clusters having pearl like arrangement of insulin monomer.

In another embodiment of the present invention, there is provided a pharmaceutical composition for the treatment of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus and complications thereof, the composition comprises therapeutically effective amount of the supramolecular insulin assembly (SIA) and/or supramolecular extendin-4 assembly (SEA) as disclosed in the present invention.

In an additional embodiment, there is provided a pharmaceutical composition for the treatment of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus and complications thereof, said composition comprising therapeutically effective amount of the supramolecular insulin assembly (SIA), wherein the assembly comprises insoluble and aggregated oligomeric form of insulin as SIA I, SIA II, SIA III stages or combination thereof, wherein SIA I consists of elongated clusters having pearl like arrangement of insulin monomer, SIA II consists of linear association of elongated clusters having pearl like arrangement of insulin monomer and SIA III consists of about 90% SIA-II, that is a dense, linear association of insulin oligomers and supramolecular extendin-4 assembly (SEA) as disclosed in the present invention.

In another embodiment, the present invention provides a pharmaceutical composition for the treatment of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus and complications thereof, said composition comprising therapeutically effective amount of the supramolecular insulin assembly (SIA), wherein the assembly comprises insoluble and aggregated oligomeric form of insulin at SIA II, wherein SIA II consists of linear association of elongated clusters having pearl like arrangement of insulin monomer and supramolecular extendin-4 assembly (SEA) as disclosed in the present invention.

One embodiment of the present invention provides the pharmaceutical composition comprising supramolecular insulin assembly of the present invention, wherein the composition upon administration releases insulin for about 7 days to 180 days.

In another embodiment, the present invention provides the pharmaceutical composition comprising supramolecular insulin assembly as claimed in any of the preceding claims, wherein said composition upon administration maintains near-normoglycemic level (120±30 mg/dl) for about 180 days in a subject in need thereof.

In yet another embodiment of the present invention there is provided the pharmaceutical composition comprising supramolecular insulin disclosed in the present invention, wherein single dose of said composition upon administration maintains near-normoglycemic level (120±30 mg/dl) for about 4-180 days in a subject in need thereof, the concentration of said assembly in said composition is in the range of 25 to 750 μg.

Further embodiment provides the pharmaceutical composition comprising supramolecular insulin assembly of the present invention, wherein single dose of said composition upon administration maintains near-normoglycemic level (120±30 mg/dl) for about 180 days in a subject in need thereof, the concentration of said assembly in said composition is in the range of 150 to 250 μg.

In this embodiment, the pharmaceutical composition comprising supramolecular insulin assembly of the present invention, wherein rate of release of insulin is in a range of 0.5-1.5 ng/ml for at least up to 180 days.

In another embodiment, there is provides a pharmaceutical composition for the treatment of osteoporosis, the composition comprising supramolecular calcitonin assembly (SCA) as disclosed in the present invention.

In another embodiment, the present invention provides the pharmaceutical composition the composition comprising supramolecular calcitonin assembly (SCA) as disclosed in the present invention, wherein said composition releases calcitonin.

In another embodiment, the present invention provides the pharmaceutical composition comprising supramolecular calcitonin assembly (SCA) as disclosed in the present invention, wherein said composition upon administration releases calcitonin for about 55 to 60 days.

In yet another embodiment, the present invention provides the pharmaceutical composition comprising supramolecular calcitonin assembly (SCA) as disclosed in the present invention, wherein single dose of the composition upon administration releases calcitonin for about 55 to 60 days, wherein concentration of calcitonin released from supramolecular calcitonin assembly (SCA) is in the range of 15-20 pg/ml.

The present invention also provides a pharmaceutical composition for the treatment of arthritis, the composition comprising supramolecular ibuprofen assembly (SIbA) of the present invention.

In one embodiment of the present invention there is provided the pharmaceutical composition the composition comprising supramolecular ibuprofen assembly (SIbA) of the present invention, wherein the composition releases ibuprofen.

In another embodiment, the present invention provides the pharmaceutical composition comprising supramolecular ibuprofen assembly (SIbA) of the present invention, wherein the composition upon administration releases ibuprofen for about 3 to 6 days.

In yet another embodiment of the present invention, there is provides the pharmaceutical composition comprising supramolecular ibuprofen assembly (SIbA) of the present invention, wherein single dose of the composition upon administration releases ibuprofen for about 3 to 6 days, wherein concentration of the supramolecular ibuprofen assembly (SIbA) is in the range of 10 to 20 mg.

The pharmaceutical composition disclosed in the present invention comprises pharmaceutically acceptable carriers, additives or diluents.

The pharmaceutical composition disclosed in the present invention is administered intravenously, intramuscularly, orally or subcutaneously.

The pharmaceutical composition disclosed in the present invention is administered through a device capable of releasing the composition, wherein the device is selected from a group consisting of pumps, catheters and implants.

The pharmaceutical composition disclosed in the present invention, wherein single dose of the composition upon administration releases said protein for prolonged period.

In accordance with the present invention, one embodiment provides a process of preparation of supramolecular insulin assembly (SIA) as disclosed in the present invention, the process comprises; dissolving insulin at a temperature of about 25 to 60° C. in a solution having pH in the range of 1.5 to 7.8; and incubating the above for a period of 6-48 hours with constant stirring to obtain Supramolecular Insulin Assembly (SIA), wherein SIA comprises insoluble and aggregated oligomeric form of insulin

In another embodiment of the present invention, there is a process of preparation of supramolecular insulin assembly (SIA) as disclosed in the present invention, wherein the process further comprises washing the SIA with PBS; and re-suspending the SIA in PBS.

In yet another embodiment of the present invention, there is provided a process of preparation of supramolecular calcitonin assembly (SCA) as disclosed in the present invention, the process comprises dissolving calcitonin at a temperature of about 25 to 60° C. in a solution having pH in the range of about 4.0 to 8.0; and incubating the above for a period of 6-48 hours with constant stirring to obtain Supramolecular Calcitonin Assembly (SCA), wherein SCA comprises insoluble and aggregated oligomeric form of calcitonin.

In a further embodiment, process of preparation of supramolecular calcitonin assembly (SCA) as disclosed in the present invention further comprises washing the SCA with PBS; and re-suspending the SCA in water or 2% mannitol

In yet another embodiment of the present invention there is provided a process of preparation of supramolecular ibuprofen assembly (SIbA) of the present invention, the process comprises dissolving peptide tagged-ibuprofen at a temperature of about 25 to 60° C. in a solution having pH in the range of about 3.5 to 7.6; and incubating the above for a period of 6-192 hours to obtain Supramolecular Ibuprofen Assembly (SIbA), wherein SIbA comprises insoluble and aggregated oligomeric form of peptide tagged ibuprofen.

In still yet another embodiment, the present invention provides the process of preparation of supramolecular ibuprofen assembly (SIbA) of the present invention, wherein the process further comprises washing the SIbA with PBS; and re-suspending said SIbA in PBS.

The present invention also provides a process of preparation of supramolecular Extendin assembly of the present invention, the process comprises dissolving extendin 4 at a temperature of about 25 to 60° C. in a solution having pH in the range of about 2.0 to 7.6; and incubating the above for a period of 6-192 hours with constant stirring to obtain Supramolecular Extendin Assembly (SEA), wherein SEA comprises insoluble and aggregated oligomeric form of Extendin-4

The process of preparation of supramolecular Extendin assembly of the present invention further comprises washing said SEA with PBS; and re-suspending the SEA in PBS.

One embodiment provides the solution for dissolving the protein, wherein the solution is selected from a group consisting of hydrochloric or acetic acid in water having pH in the range of 1.5 to 2.5; sodium acetate buffer having pH in the range of 3.5 to 5.5; phosphate buffer (PBS) having pH 6, and citrate buffer having pH in the range of 4 to 6.

The process of preparation of supramolecular protein assembly disclosed in the present invention comprises dissolving the protein at 37° C. temperature.

The process of preparation of supramolecular protein assembly disclosed in the present invention comprises dissolving the protein in a solution having pH 7.2.

The process of preparation of supramolecular insulin assembly disclosed in the present invention comprises incubation of the insulin in the solution for 10 hours.

The process of preparation of supramolecular calcitonin assembly disclosed in the present invention comprises incubation of the calcitonin in the solution for 8 hours.

The process of preparation of supramolecular ibuprofen assembly disclosed in the present invention comprises incubation of the ibuprofen tagged with peptide in the solution for 32 hours.

The process of preparation of supramolecular protein assembly disclosed in the present invention comprises incubation of the protein in the solution for 6-192 hours.

The present invention further provides a method for treating metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus or chronic diseases selected from a group consisting of osteoporosis, arthritis, cancer, endotoxic shock, wherein the method comprising administering to a subject in need thereof a therapeutically effective amount of the pharmaceutical composition disclosed in the present invention, which is effective for the alleviation of the disorder or disease.

In one embodiment, the present invention provides a method for treating metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus, wherein the method comprising administering to a subject in need thereof a therapeutically effective amount of the pharmaceutical composition comprising the supramolecular insulin assembly of the present invention, which is effective for the alleviation of the disorder or disease.

In another embodiment of the present invention, there is provided a method for treating osteoporosis, wherein the method comprising administering to a subject in need thereof a therapeutically effective amount of the pharmaceutical composition comprising the supramolecular calcitonin assembly disclosed in the present invention, which is effective for the alleviation of osteoporosis.

In yet another embodiment of the present invention there is provided a method for treating arthritis and arthritic pain, wherein the method comprising administering to a subject in need thereof of a therapeutically effective amount of the pharmaceutical composition comprising supramolecular ibuprofen assembly of the present invention which is effective for the alleviation of arthritis and arthritic pain.

The method for treatment using the pharmaceutical composition as disclosed in the present invention, wherein the composition is administered intramuscularly, intra peritonealy or subcutaneously.

In accordance with the present invention, there is provided use of supramolecular insulin assembly of the present invention for the treatment of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus or chronic diseases selected from a group consisting of osteoporosis, arthritis, arthritic pain, cancer and endotoxic shock.

Further, in one embodiment of the present invention, there is provided use of supramolecular insulin assembly of the present invention for the treatment of metabolic disorders selected from the group consisting of type 1 and type 2 diabetes mellitus.

The present invention also provides use of supramolecular calcitonin assembly disclosed in the present invention for the treatment of osteoporosis.

The present invention provides use of supramolecular ibuprofen assembly as disclosed in the present invention for the treatment of arthritis and arthritic pain.

In still another embodiment, the present invention provides a composition comprising of the supramolecular protein assembly which is stable, protease resistant and has longer shelf life.

In still another embodiment, the present invention provides a composition comprising of the Supramolecular peptide tagged assembly which is stable, protease resistance and has longer shelf life.

In still another embodiment, the present invention provides a composition comprising of the supramolecular protein assembly which is stable, protease resistance and has longer shelf life ranging from about 10 days to 150 days or more.

Also within the scope of the present invention is a variety of supramolecular protein or peptide assembly (SPA), wherein the SPA comprises the insoluble and aggregated oligomeric form of the protein or peptide, wherein the protein or peptide is useful as therapeutic protein.

Any protein or peptide that can form the supramolecular protein assembly (SPA) as disclosed the present invention is within the scope of the present invention.

Further, any protein or peptide that can form the supramolecular protein assembly (SPA) by the process disclosed in the present is within the scope of the present invention.

As will be appreciated by those in the art a variety of the solutions such as known buffers can be used for re-suspension and washing of the supramolecular protein assembly disclosed in the present invention.

The term “therapeutically effective amount” as used herein refers to an amount of a therapeutic agent to treat, ameliorate, or prevent a desired disease or condition, or to exhibit a detectable therapeutic or preventative effect. The precise effective amount for a subject will depend upon the subject's size and health, the nature and extent of the condition, and the therapeutics or combination of therapeutics selected for administration. The effective amount for a given situation is determined by routine experimentation and is within the judgment of the clinician.

For purposes of the present invention, an effective dose of SIA will generally be from about 0.1 mg/kg to about 1.0 mg/kg, or about 0.2 mg/kg to about 2.0 mg/kg or about 0.5 mg/kg to about 3.0 mg/kg of the compositions of the present invention in the subject to which it is administered.

For purposes of the present invention, an effective dose of SCA will generally be from about 0.1 mg/kg to about 0.3 mg/kg, or about 0.3 mg/kg to about 0.8 mg/kg or about 0.5 mg/kg to about 1.0 mg/kg of the compositions of the present invention in the subject to which it is administered.

For purposes of the present invention, an effective dose of SIbA will generally be from about 2.0 mg/kg to about 10.0 mg/kg, or about 10.0 mg/kg to about 15.0 mg/kg or about 15.0 mg/kg to about 30.0 mg/kg of the compositions of the present invention in the subject to which it is administered.

For purposes of the present invention, an effective dose of SEA will generally be from about 0.1 mg/kg to about 0.5 mg/kg, or about 0.5 mg/kg to about 1.0 mg/kg or about 1.0 mg/kg to about 3.0 mg/kg of the compositions of the present invention in the subject to which it is administered.

A pharmaceutical composition can also contain a pharmaceutically acceptable carrier. The term “pharmaceutically acceptable carrier” refers to a carrier for administration of a therapeutic agent, such as antibodies or a polypeptide, genes, and other therapeutic agents. The term refers to any pharmaceutical carrier that does not itself induce the production of antibodies harmful to the individual receiving the composition, and which can be administered without undue toxicity. Suitable carriers can be large, slowly metabolized macromolecules such as proteins, polysaccharides, polylactic acids, polyglycolic acids, polymeric amino acids, amino acid copolymers, and inactive virus particles. Such carriers are well known to those of ordinary skill in the art. Pharmaceutically acceptable carriers in therapeutic compositions can include liquids such as water, saline, glycerol and ethanol. Auxiliary substances, such as wetting or emulsifying agents, pH buffering substances, and the like, can also be present in such vehicles. Typically, the therapeutic compositions are prepared as injectables, either as liquid solutions or suspensions; solid forms suitable for solution in, or suspension in, liquid vehicles prior to injection can also be prepared. Liposomes and neosomes are included within the definition of a pharmaceutically acceptable carrier. Pharmaceutically acceptable salts can also be present in the pharmaceutical composition, e.g., mineral acid salts such as hydrochlorides, hydrobromides, phosphates, sulfates, and the like; and the salts of organic acids such as acetates, propionates, malonates, benzoates, and the like.

The pharmaceutical compositions can be prepared in various forms, such as granules, tablets, pills, suppositories, capsules, suspensions, salves, lotions and the like. Pharmaceutical grade organic or inorganic carriers and/or diluents suitable for oral and topical use can be used to make up compositions containing the therapeutically-active compounds. Diluents known to the art include aqueous media, vegetable and animal oils and fats. Stabilizing agents, wetting and emulsifying agents, salts for varying the osmotic pressure or buffers for securing an adequate pH value, and skin penetration enhancers can be used as auxiliary agents.

The pharmaceutical compositions disclosed in the present invention are useful for the treatment of metabolic disorders particularly diabetes, and other chronic and inflammatory diseases such as rheumatoid arthritis, osteoporosis, chronic inflammatory and peripheral pain, sepsis, and allergy where a continuous and prolonged therapy is required using peptides, proteins or small drug molecules.

The compositions disclosed in the present invention comprise supramolecular protein assemblies of the relevant/applicable therapeutic proteins and are applicable for treatment of a number of chronic diseases and acute symptoms.

The compositions disclosed in the present invention comprises oligomers of therapeutic proteins particularly the supramolecular assembly of a protein for sustained release of the protein.

Some widely-used biopharmaceuticals such as insulin, glucagon, and calcitonin can be induced to form amyloids. Compared to soluble precursor proteins, amorphous aggregates formed as a prelude to amyloid formation, gain new properties such as enhanced stability, protease resistance; self-propagation, longer shelf life, highly organized structure and can serve as a concentrated compact source of pure molecules.

The supramolecular protein assemblies disclosed in the present invention exist with in a defined structure having both α-helical and β-sheet components. The adoption of the above mentioned unique structure results in a change in its solubility and its structure from the native insulin molecules in solution. Significantly, release of insulin monomers from this supramolecular structure are biologically active and thus resemble the native insulin structure. Novel dissolution properties are conferred upon this supramolecular structure formed, which acts as a prodrug, as by itself viz. In its prodrug form it was found that it has no action or effect on the signaling events or glucose homeostasis of the insulin sensitive fat cells. It is transformed into a drug by the release of insulin monomers from the depot or site of injection in vivo. Both in vitro and in vivo results demonstrate the uniqueness of the formulation to release bioactive insulin molecules showing an effect on the glucose homeostasis and other clinical parameters usually assessed for type I and II diabetes.

The present invention provides a composition comprising supramolecular insulin assembly useful in the treatment of diabetes mellitus. Supramolecular insulin is a hybrid of amorphous and nascent fibrillar oligomers of insulin and serves as a sustained release formulation for the release of bioactive insulin. The glucose regulatory hormone insulin is a 51 residue polypeptide that exists in equilibrium as a mixture of different oligomeric states, including hexamers, dimers and monomers, depending on the environment. In pancreatic secretory vesicles, insulin is stored as a hexamer at physiological pH, whereas it interacts with its receptor as a monomer. Under denaturing conditions, such as low pH or in the presence of strong denaturants, insulin aggregates to form amyloid fibrils (Paul Bevan Insulin signalling. J. Cell Sci., 114, 1429-1430 (2001)).

One embodiment of the present invention provides a process for preparation of supramolecular oligomers of protein for the treatment of various diseases, like metabolic disorders particularly diabetes. The inventors also lay claim on other acute and chronic diseases such as osteoporosis, inflammatory and chronic pain, rheumatoid arthritis, arthritic pain, cancer, endotoxic shock, etc where a similar approach to transform the peptide or present the drug molecule attached to such a transformed supramolecularly oligomerized proteins or peptides' and use them as a depot of the native drug has given good results.

The supramolecular oligomers of insulin disclosed in the present invention is prepared at a pH ranging from 6.8 to 7.8 preferably 7.2.

The present invention provides a composition comprising supramolecular insulin assembly capable of sustained release of insulin monomers. The composition comprising a given supramolecular insulin assembly (viz SIA I, II III or a combination thereof) is useful for achieving better glycemic control.

The present invention provides insulin oligomers, supramolecular insulin assembly II that is useful in achieving tighter glycemic control by achieving a sustained release of insulin. Supramolecular insulin assembly II when administered subcutaneously or intramuscularly maintains a basal level of insulin in STZ induced diabetic rat for a prolonged period ranging from about 10 days to 180 days or more, while simultaneously keeping a tight glycemic control, thus affording a long lasting treatment against diabetes mellitus.

According to the present invention, one embodiment provides a composition comprising supramolecular insulin assembly II that causes a sustained release of insulin monomers ranging between 0.5-1.5 ng/ml and lasts about at least 180 days when administered intramuscularly or subcutaneously.

Another embodiment of the present invention provides that the composition comprising supramolecular insulin assembly II wherein the amount of insulin monomer released from the supramolecular insulin assembly II is in the range of 0.5-1.5 ng/ml in serum.

In an embodiment of the present invention, the in-vivo effect of the composition comprising supramolecular oligomers of insulin on controlling blood glycemic levels have been verified using STZ induced diabetic rats.

Another embodiment of the present invention provides the dosage of the composition comprising supramolecular insulin assembly wherein the dosage ranging from about 50 μg to about 400 μg of insulin was monitored for the experimental time period.

Another embodiment of the present invention provides the dosage of the composition comprising supramolecular insulin assembly wherein the dosage is 200 μg of insulin.

Another embodiment of the present invention provides the dosage of the composition comprising supramolecular insulin assembly wherein the dosage is 100 μg of insulin.

In still another embodiment of the present invention provides a composition comprising the supramolecular insulin assembly, wherein the composition does not elicit insulin degrading enzyme activity (IDE) in and around the site of injection for a time period ranging from about 10 days to 180 days or more.

In yet another embodiment of the present invention, there is absence of anti-insulin antibodies in the serum of the subject for a time period of ranging from about 10 days to 150 days or more.

In still another embodiment, the present invention provides a composition comprising of the supramolecular insulin assembly which is stable, protease resistance and has longer shelf life ranging from about 10 days to 150 days or more.

In yet another embodiment of the present invention, a composition comprising the supramolecular insulin assembly which is capable of releasing insulin monomers in a controlled manner for a long period of time without any burst of rapid release. The kinetics of transformation can be controlled both in vivo and in vitro.

Further, a composition comprising the supramolecular insulin assembly disclosed in the present invention can be used as a single dose having long lasting effect that frees the patients from the need to administer multiple doses of insulin every day.

The composition comprising the supramolecular insulin assembly disclosed in the present invention does not exhibit an abrupt large release of insulin thwarting hypoglycemic stage in diabetic subjects.

The composition comprising the supramolecular insulin assembly disclosed in the present invention is capable of releasing insulin monomers at a constant rate both in vitro and in vivo.

In still another embodiment of the present invention, the higher oligomeric stage of the supramolecular insulin assembly achieves a tightly regulated glycemic control without fasting hypoglycemia in diabetic subject.

In still another embodiment of the present invention, the higher oligomeric stage of the supramolecular insulin assembly achieves a tightly regulated glycemic control without fasting hypoglycemia in Type 1 diabetic subject.

In still another embodiment of the present invention, the higher oligomeric stage of the supramolecular insulin assembly achieves a tightly regulated glycemic control without fasting hypoglycemia in Type 2 diabetic subject.

In yet another embodiment of the present invention, there is no sudden increase of body weight of subjects when treated with the supramolecular insulin assembly or composition comprising supramolecular insulin assembly of the present invention.

In still another embodiment of the present invention, no lag phase is found in the release of bioactive insulin monomers from the supramolecular insulin assembly II in the Intraperitoneal Glucose Tolerance Test (IPGTT) blood glucose profile of the subject, similar to the administration of free insulin.

In yet another embodiment of the present invention, zero order kinetics or sustained release is observed for in vivo release of insulin monomers from the supramolecular insulin assembly II.

In still another embodiment of the present invention, insulin released from the supramolecular insulin assembly II is equivalent in biological function to soluble insulin.

Further, in another embodiment of the present invention, toxicity of the supramolecular insulin assembly is ruled out by performing biological assays for Serum glutamate oxalo-acetate transaminase (SGOT), serum glutamate pyruvate transaminase (SGPT), total Bilirubin, Bilirubin, Alkaline Phosphatase, Serum total proteins, Serum Albumin, Serum Globulin, Serum A/G ratio, Kidney function test (KFT), Cataract Formation, Adipose Tissue weight, Body Weight and appearance.

In yet another embodiment, the rate of glucose infusion remains the same in treated animals. This concludes that the monomers released from the depot at the site of injection are biologically active and stimulate the muscles and the liver to take up glucose.

In still another embodiment, MTT assay was performed on MCF 7 cells to validate the unchanged structural and binding dynamics of the insulin monomers, released from SIA II.

Further, in another embodiment of the present invention, male Wistar rats were rendered diabetic using another chemical compound Alloxan. These diabetic rats were further treated with SIA II and showed similar result to that of STZ induced diabetic rat. A tight glycemic control was observed.

In still another embodiment of the present invention, C57BL/6 mice were made diabetic using streptozotocin, thereafter treated with SIA II, also showed normo-glycemic levels.

Another embodiment of the present invention is that the supramolecular insulin assembly is a stable depot useful for the controlled release of active peptide drugs from the supramolecular insulin assembly termini.

According to one embodiment of the present invention the supramolecular insulin assembly II is capable of affording a long lasting treatment against diabetes.

In another embodiment, the insulin used for preparation of supramolecular insulin assembly is preferably recombinant human insulin, bovine and pig insulin.

In still another embodiment, the composition comprising the supramolecular insulin assembly I and II (SIA I and II) or a combination thereof, disclosed in the present invention is capable of lowering blood glucose levels in animal subjects treated with streptozotocin to induce type II diabetes.

Another embodiment of the present invention utilizes the formation of oligomeric assembly by Exendin 4, tagged with a peptide sequence of G-N-N-Q-Q-N-Y at the C-terminus (termed Exendin 4a), as an adjunct therapy for the treatment of Type II Diabetes along with supramolecular insulin assembly (SIA I and II).

Further, in another embodiment of the present invention, a supramolecular oligomeric complex was formed with Exendin 4.

In still another embodiment, SIA I, which releases insulin monomers at a faster rate was administered to rats suffering from Diabetes Mellitus Type II (DM II).

According to one embodiment of the present invention, SIA II was also administered to DM II rats for the treatment.

In yet another embodiment, diabetic rats treated with both SIA I and II showed near normoglycemic levels bordering on the higher side, in both pre-prandial and post-prandial (180±15 mg/dl) states.

In yet another embodiment of the present invention, the dosage of SIA II injected was 150 μg in two places, both subcutaneously and intramuscularly.

Another embodiment of the present invention demonstrates the ability of SIA I and II to maintain near normoglycemic levels for up to 30 days.

In still another embodiment, administration of Exendin 4a along with insulin therapy was able to maintain near normoglycemic levels (135±10 mg/dl) for up to 45 days, and was a better formulation for treating DM II.

Further in another embodiment, SIA III, which releases insulin monomers but at a very slow rate (0.05-0.3 ng/ml) which can be useful in the treatment of borderline diabetic patients, viz prediabetic or subjects with poor prognosis in glucose tolerance tests) who require very little amount of insulin as a therapy.

In yet another embodiment of the present invention, the level of human insulin detected in the serum of diabetic rats is about 0.7-0.85 ng/ml.

In still another embodiment of the present invention, various serum parameters were estimated, such as triglycerides (TAG), free fatty acids (FFA), to demonstrate the effectiveness of the treatment.

In yet another embodiment, the level of TAG in the serum was in the range of 0.45-0.6 mmol/l for the insulin SIA+Exendin 4a treated rats, which is almost same to the control.

Further in another embodiment, the FFA levels in the serum was estimated to be about 0.85-0.9 mmol/l for the insulin SIA+Exendin 4a treated rats, which is almost same to the control.

In still another embodiment of the present invention, the increase in the body weight of the treated animals was almost same as that of control rats.

In yet another embodiment, the current methodology can be extended to those chronic and inflammatory diseases where a sustained and continuous therapy is required using peptides, proteins or small molecules.

Another embodiment of the present invention relates to the formation of supramolecular assembly of calcitonin, exendin 4 and the peptide GNNQQNY tagged ibuprofen, and its therapeutic utilization for the treatment of various diseases.

In still another embodiment of the present invention, supramolecular oligomer of salmon calcitonin was used for the treatment of osteoporosis in diseased subjects.

According to one embodiment of the present invention, the formation of amyloid fibrils by salmon clacitonin is concentration dependent and is completely formed by 44 h.

In yet another embodiment, the supramolecular calcitonin assembly (SCA) I, II and III are formed by 6, 8 and 12 h respectively.

Further, in another embodiment of the present invention, the release of free calcitonin from SCA follows a bell shaped curve (in small volume) like that of insulin, with continuous release through a dialysis membrane (in large volume of aqueous solvent).

In still another embodiment of the present invention, the release of calcitonin monomers from fully grown fibrils was negligible.

In yet another embodiment of the present invention, the supramolecular calcitonin assembly (SCA) was incorporated into Alzet pumps, from which a slow and controlled release of calcitonin monomers at a rate of 2.5 Oh is obtained.

According to one embodiment of the present invention, ovariectomised rats were administered vehicle or human/salmon calcitonin either intermittently by subcutaneous injection or continuously by Alzet osmotic minipumps containing 200 μl of either Calcitonin (CT) or supramolecular calcitonin assembly (SCA, 2 mg/ml) in 2% mannitol.

In still another embodiment, a dosage of 8 U/kg b wt was given to ovariectomised rats through the pump and 16 U/kg b wt subcutaneously on alternate days.

In yet another embodiment, demeclocycline and calcein was administered 10 and 3 days before sacrifice, respectively, at a dosage of 15 mg/kg b wt.

According to one embodiment of the present invention, the serum levels of calcitonin was maintained at a higher level (19 pg/ml) in rats treated with SCA compared to that of other groups.

In still another embodiment of the present invention, the serum level of calcitonin was maintained at a higher level for up to 60 days with a single pump containing the SCA.

In yet another embodiment of the present invention, supramolecular calcitonin treated rats' demonstrated marginal increase in their body weight, calcium and phosphorous levels, in comparison to ovariectomised rats given vehicle which had an increase in their body weight by almost 11% during the experimental time frame and an increase in calcium and phosphorous levels in serum.

Further, in another embodiment of the present invention, negligible levels of antibodies were found against salmon calcitonin in the serum of the treated animals.

Example 1 of the present invention provides a process for preparation of supramolecular insulin assembly II. The figure provides details of the insulin (both human and bovine) fibril formation monitored by using Thioflavin T (Th-T) fluorescence (Le Vine, H. Quantification of β-Sheet Amyloid Fibril Structures with Thioflavin T. Methods Enzymol 309, 274-284 (1999)). Fibril formation by bovine insulin was noted by acquisition of Th-T fluorescence, when the insulin was agitated at 180 rpm at 37° C., both at pH 7.0 (50 mM PBS) and pH 2.0 (hydrochloric acid in water) (FIG. 1). The increase in Th-T fluorescence occurred due to its binding to insulin fibrils reaching a maximum value at 48 hrs for insulin incubated at pH 7.0, while at pH 2.0 the fibril formation is rapid and therefore, Th-T fluorescence attained a maximum value at 20 hr. FIG. 1 compares the fibril formation by both bovine and human insulin.

Example 2 of the present invention provides kinetics of the release of insulin monmers from supramolecular insulin assembly-II. The supramolecular insulin assembly form of insulin acts as a reservoir for the sustained release of insulin monomer for a long time (FIG. 2 a). The release of insulin monomers from its amyloid and various supramolecular assemblies of insulin were noted and is depicted by FIG. 2 b&c. The fully formed amyloid fibers release negligible insulin irrespective of pH. At pH 2.0, supramolecular insulin assembly intermediates, particularly, supramolecular insulin assembly II, release insulin at a very slow rate suggesting that these oligomers are sturdy and tightly associated. However, the pH 7.0 intermediate (termed supramolecular insulin assembly II), exhibiting a turbidity of 0.9-1.3 at 600 nm, release insulin at an appreciable rate. A linear increase in the release of insulin monomers at 280 nm absorbance over a period of 15±5 days is observed. When insulin release from SIA was observed under constant volume of 1 ml, a bell shaped curve was observed (FIG. 2 d). This demonstrates the reversibility of the oligomer formation procedure and the existence of equilibrium between free insulin and SIA. The tyrosine fluorescence of the released sample corroborated these observations as is provided in FIG. 2 a. The insulin amyloid intermediate, supramolecular insulin assembly II (alternatively called insulin pre-amyloid II) meets the requirement of a sustained release of 2-4 μM (0.4-0.6 IU) of insulin monomers per hour in vitro, thereby achieving a constant yet slow release in vivo for maintaining basal insulin levels in the body.

Example 3 provides characterization of supramolecular insulin assembly using Congo-Red (CR) binding (Klunk, W. E., Jacob, R. F. & Mason, R. P. Quantifying amyloid by Congo red spectral shift assay. Methods Enzymol 309, 285-305 (1999)). Like Th-T, CR also binds specifically to the β-sheet rich structures of amyloid and has been used routinely for their detection. CR binding to samples incubated with 50 μM CR in PBS for 1 h at 37° C. was monitored by the red shift in its absorption maximum by scanning 400-600 nm regions. FIG. 3 provides that the supramolecular insulin assembly (rH and bovine) exhibits weak binding to CR, whereas fully grown fibers at pH 2.0 and 7.0 showed significant binding.

Example 4 Supramolecular insulin assembly I, II and III were also characterized using ATR-FTIR. Distinct spectra corresponding to each stage was observed (FIG. 4). A shift of the IR band towards lower frequencies is observed. Supramolecular insulin assembly II has a sharp peak at 1647-1645 cm⁻¹, while the fully formed insulin fibril (amyloid) has a peak at 1630-1628 cm⁻¹ for bovine and rH insulin respectively. The FTIR spectra of Supramolecular insulin assembly II is in good agreement with the CR data showing that the protein is still largely helical, albeit with an increase in the content of random coil structure.

Morphology of fibers formed at pH 2.0 and 7.0 were assessed by Atomic Force Microscopy (AFM) and Transmission Electron Microscopy (TEM) as provided in Example 5 and 6. Native insulin molecules (both bovine and rH) at pH 7.0 and pH 2.0 show random distribution with a height of 1.3±0.21 nm, which correlates with the dimension of insulin monomers (1.11 nm) and dimers (1.49 nm) (FIG. 5 a). Intermediates of the fibrilization process at pH 7.0 are shown in FIG. 5( b-d) for bovine insulin and FIG. 5( e-g) for rH insulin. SIA-I represent elongated clusters having a pearl-like arrangement. In between, there are some elongated linear particles with 12±2 nm heights, suggesting further association into higher oligomeric states. The SIA-II intermediate is seen as a linear association of the above mentioned elongated clusters in case of both bovine and rH insulin, having a unique entity with a supra-oligomeric structural organization (FIG. 5( c and e)). SIA-III (fibril stage succeeding SIA-II) showed an increase in density of higher oligomeric structures. Fully grown fibers at pH 7.0 represent the typical cross 13 structure of insulin amyloid (FIG. 5 h). Intermediates of pH 2.0 fibrilization process at 6-7 h reveal a lateral association of two fibrils of height 7.2-8.3 nm, and after 20 h, large twisted fibers of 10-12 nm width were observed (FIG. 5( i&j)).

Example 6 provides Transmission Electron Microscopy (TEM) to assess the presence of the possible assemblies of insulin. TEM micrographs shows the presence of some amorphous and higher oligomeric structures in the supramolecular insulin assembly II stage (FIG. 6 a). The stages after supramolecular insulin assembly II (FIG. 6 b) have more fibrillar structure as shown in (FIG. 6( c&d)). In contrast, there is an abundance of fibrillar forms when insulin was incubated at pH 2.0 [FIG. 6( e)].

Example 7 provides details of the animal models used for studying the effectiveness of insulin amyloid and supramolecular insulin assembly forms. The authors have used four different diabetes models for testing the hypothesis and the therapeutic potential of SIA, in the treatment of diabetes, namely, (a) STZ treated rats, (b) Alloxan treated rats and (c) STZ treated mice (d) STZ rabbit

To standardize the dosage, 50 μg, 100 μg, 200 μg and 400 μg of supramolecular insulin assembly-II was injected subcutaneously and alternatively intramuscularly in diabetic rats. As summarized in FIG. 7 a&b, a single dose of 50 and 100 μg of supramolecular insulin assembly maintained near-normoglycemic levels up to only 10 and 30 days respectively, compared to 135 and 160 days when 200 μg supramolecular insulin assembly, both bovine and human respectively was used. In case of 400 μg dosage, sudden non-fasting normoglycemia and fasting hypoglycemia was observed irrespective of the route used, suggesting release of an initial bolus of a basal level of insulin monomer from the SIA depot of bovine insulin. The usage of 200 μg of supramolecular insulin assembly as a therapeutic dosage was chosen for the detailed long term prospective studies.

Example 8 provides the treatment of the diabetic animals with supramolecular insulin assembly form of insulin. The STZ-induced diabetic rats assigned to multiple groups were treated with insulin (4 IU/kg, IP), supramolecular insulin assembly (200 μg both SC and IM), respectively, to study the in vivo effect of the supramolecular insulin assembly therapy on controlling blood glycemic levels. In addition, one group of PBS treated diabetic rats and another group of normal rats served as diabetic and non-diabetic control. The pre-prandial and post-prandial blood glucose levels of the rats were monitored for a period till the physiological effect of insulin was observed. As shown in FIG. 8 a&b, treatment with 200 μg of supramolecular insulin assembly maintained the basal level of insulin by the sustained and slow release of insulin monomers from supramolecular insulin assembly depot in STZ-induced diabetic rats, leading to a significant reduction in the non-fasting blood glucose levels without fasting hypoglycemia (FIG. 9 a&b). No significant difference was observed whether supramolecular insulin assembly was injected via subcutaneous or intramuscular route. In the case of free insulin (viz. in its normal counterpart; non-supramolecularly organized form) treatment (single dose of 4 IU/kg), daily blood glucose was reduced to a non-fasting value of 350-450 mg/dl and fasting 300-400 mg/dl only. Diabetic rats were given insulin intraperitoneally everyday maintained hyperglycemic blood glucose levels (300±100 mg/dl). In contrast to free insulin treatment, where daily dose was required to keep blood glucose from plummeting to very high levels, single injection of supramolecular insulin assembly was sufficient for achieving near-normoglycemia levels (150±60 mg/dl) in diabetic rat for 3 months without fasting hypoglycemia (90±50 mg/dl). Similar results were obtained with supramolecular insulin assembly formed from human insulin, as depicted in FIG. 8 b&9 b. Administration of insulin amyloid, formed at pH 7.0 and 2.0, had no beneficial effect on the glycemic status of diabetic rats, as evident from FIG. 10. Again the body weight which is an indicator of normal health was monitored along with BGL in all cases over the entire period of treatment. As shown in FIG. 11, there was an initial loss of body weight immediately after STZ treatment, but progressive weight gains were achieved in diabetic rat after treatment with supramolecular insulin assembly II and the curve of supramolecular insulin assembly treated animals paralleled that of non-diabetic control. Thus, the surprising efficacy of supramolecular insulin assembly II for use in long term treatment of diabetes mellitus is considered an improvement over the conventional methods.

Example 11 provides intraperitoneal glucose tolerance test to assess the efficacy of supramolecular insulin assembly to release insulin in a continuous manner. The in vivo release of insulin was monitored. The biological activity of the released monomer was estimated by blood glucose disposal from the blood. The details of the independent experiments performed are shown in FIG. 12. The glucose levels were determined before (T_(o)) and 30, 90, 150, 270 and 330 min after glucose administration to fasting normal and STZ treated rats, upon treatment with PBS, supramolecular insulin assembly II and insulin. As shown in FIG. 12, insulin injection, supramolecular insulin assembly II treatment or in vitro released monomers alone significantly improved the glucose tolerance test in treated animals, and their elevated blood glucose levels after the glucose infusion returned to the pre challenged levels within 1.5 hrs.

Example 12 describes serum insulin quantification of bovine and rH insulin on administering supramolecular insulin assembly (FIG. 13 a). Serum insulin was detectable up to a period of 150 and 180 days for bovine and rH insuline SIA-II, respectively, which corresponded to a decrease in BGL. The decrease in blood glucose levels was sustained up to a period of 150 and 180 days for bovine and rH insuline SIA-II, respectively, maintaining near normal glucose values for more than 20-25 weeks with a single dose of the supramolecular insulin assembly II. Solid state ELISA was performed to quantify the plasma levels of insulin released from the insulin SIA II, which is responsible for the maintenance of normal blood glucose values. As expected, basal or slightly above basal level insulin release was achieved in case of supramolecular insulin assembly treated diabetic rats (0.5-1.2 ng/ml) compared to non-detectable insulin level (0.08 ng/ml) in PBS treated diabetic rats (FIG. 13 a&c). A sustained release of insulin (0.8-1.1 ng/ml) was observed from the day of injection up to 150-180 days irrespective of the route, which contributed to near-normoglycemic values in the supramolecular insulin assembly treated animals. While some variation was seen from animal to animal, remarkable values of insulin release could be achieved ranging from 0.5-1.2 ng/ml. This basal level was enough to maintain normo-glycemic levels up until the exhaustion of the supramolecular insulin assembly. However, in insulin treated diabetic animals, a relatively higher mean serum level was detected, but with high degree of variation between animals. This was attributable to inter-subject variability in BGL by insulin treatment alone. Serum insulin levels were also quantified for the glucose tolerance test performed, for which glucose data has already been shown. FIG. 13 b, describes the bovine insulin values in the serum of rats up to 270 min in IPGTT experiments. In case of both control and STZ treated rats given PBS only, the bovine insulin value is almost negligible (FIG. 13 b). Whereas, in case of insulin administration, the insulin values increases to ˜0.9 ng/ml in 30 min, and then decreases over a period of time. Similar profile was observed when terminally released insulin which is equivalent to free insulin was used. This corresponds to the decrease in blood glucose levels, followed by its increase due to uptake and degradation of insulin. On the other hand, in supramolecular insulin assembly treatment, insulin levels in serum reached to 0.8-0.9 ng/ml, equivalent to the basal level in 30 min and then remained constant over the period of study, as seen by bovine insulin quantification. This sustained basal level ensures a normo-glycemic level, instead of decreasing the levels drastically and making the animal hypoglycemic. Further, Rat insulin ELISA was performed to evaluate the serum insulin levels for both control rats and STZ treated ones. As shown in FIG. 13 c, rat basal insulin levels is 0.501 ng/ml and increases manifold in response to infused glucose. In case of STZ treated rats, basal insulin levels are almost negligible, due to the destruction of the pancreatic β cells by STZ. This confirms that the decrease in blood glucose levels seen in case of supramolecular insulin assembly treatment is due to the release of bovine/rH insulin released from the SIA II. In the process of preparation of insulin SIA II, insulin other than bovine and rH insulin selected from a group consisting of but not limited to pig insulin is employed.

Example 13 provides I¹²⁵ labeling of insulin to validate and quantify the in vitro release from the termini of SIA II. Supramolecular insulin assembly II formed from labeled insulin has a specific activity of 49912 CPM/ml/μg. 50 μl of supramolecular insulin assembly (4991200 CPM) was injected subcutaneously as well as intramuscularly and blood glucose levels were monitored and serum samples were collected at 0, 30 min, 1 h, 4 h, 10 h, 24 hrs, thereafter once a day, and then on alternate days or once in a week. Counts in per ml of serum were measured (FIG. 14 a). As shown, blood glucose profile was same as observed with unlabeled SIA II. The CPM/ml calculated remained almost constant (FIG. 14 a) when plotted against number of days of treatment. However there was an initial high count at 30 min-4 hrs, which then gradually decreased to constant level of 2000-3000 in 10 hrs. The amount of insulin released in blood was calculated and was in the range of 0.5-1.2 ng/ml which corresponds to the basal or slightly above basal level of insulin in the serum as observed with ELISA (FIG. 14 b). To further prove that released insulin from supramolecular insulin assembly is monomeric, serum of different time points were resolved on tricine-SDS-PAGE and radiogram was developed using the phosphor imager. As shown in FIG. 15, the band in serum corresponds to free insulin monomer and its intensity remained constant for a long period when equal amount of serum was loaded. A decrease in intensity was observed after 20 days showing usage and depletion of the supramolecular insulin assembly depot over a period of time together with some effect of the decay of the radio-label itself.

Example 14 describes hyperglycemic clamp studies performed to assess the slow and continuous release of insulin monomers from the injected SIA II. At one week, one month and three month time interval, the rate of glucose infused for maintaining hyperglycemic state remained unchanged during the course of the experiment. This shows that there is constant insulin release from the depot at the site of injection. In case of the group being administered free insulin, the amount of glucose infused decreases over time, which is due to a decrease in the uptake of blood glucose by muscle and liver in the absence of continuous supply of free insulin (FIG. 16 a-c).

Example 15 provides the effect of insulin on glucose transport and other metabolic events in adipose tissues that are mediated by intracellular signaling cascades which start after insulin binds to insulin receptors on cell surface (Paul Bevan Insulin signalling. J. Cell Sci., 114, 1429-1430 (2001)). The effect of insulin in the cell is mediated by the activation of intracellular mediators like PI3K, AKT and ERK. Activation of the PI3 kinase and Akt, mediates insulin induced glucose uptake and GLUT-4 vesicle translocation to the plasma membrane and is involved in various other insulin effects including inhibition of lipolysis and activation of fatty acid, glycogen, protein and DNA synthesis. On the other hand, activation of the extracellular signal-regulated kinase (ERK) pathway is implicated in mitogenic responses of pre-adipocytes to growth factors. The level of PI3K which is the first kinase downstream to insulin signaling was studied. As shown in FIG. 17 a, the level of PI3K is augmented significantly when supramolecular insulin assembly and insulin released in vitro from them is used compared to control. There was no significant difference observed compared to insulin. The total protein and activated level of Akt, a threonine/serine kinase important for regulation of insulin action and its various metabolic responses in adipocytes was also assessed. A significant increase in p-Akt level was observed which was again similar to the response observed with free insulin. There was no difference in total Akt protein level hence, no difference in its expression in the presence of insulin or its supramolecular insulin assembly II was observed. To assess whether the observed temporal profiles and level of Akt phosphorylation in adipocytes was parallel to the difference in Akt activity, the phosphorylation of the endogenous Akt substrate GSK3β was monitored by immunoblotting using antibodies to GSK3β and p-GSK3

GSK3

is directly phosphorylated by Akt on ser-21 and is inactivated following its phosphorylation. The phosphorylation of GSK3

increased several fold in adipocytes treated with either free insulin or supramolecular insulin assembly II compared to control and there was no significant difference among the treated cells. No difference was observed in total GSK3

protein level suggesting no change in its expression subsequent to treatment. Therefore, both Akt and GSK3

showed rapid and pronounced responses to supramolecular insulin assembly II and released insulin from supramolecular insulin assembly and were similar to responses observed in stimulation with free insulin used as a control. The activation of ERK in treatment with supramolecular insulin assembly and insulin released from it in adipocytes was observed, as this kinase is involved in insulin-mediated regulation of adipocytes transcription factors and adipose tissue development. On treatment of adipocytes with insulin, supramolecular insulin assembly and released insulin from supramolecular insulin assembly, a significant activation of ERK 1/2 was observed compared to control. The phosphorylation of ERK 2 was two fold higher than ERK 1 suggesting more expression of ERK 2 on treatment. There were no significant difference in phosphorylation pattern of ERK 1/2 in SIA, insulin or serum treated cells. Therefore the ERK phosphorylation in supramolecular insulin assembly II and insulin treated cells were similar in the context of PI3K, Akt and GSK3

mediated signaling. Similar activation of signaling mediators was observed, when serum from insulin or its SIA-II treated animals was added to cultured adipocytes (FIG. 17 b) Together these data demonstrate that insulin released from supramolecular insulin assembly II is able to activate the insulin signaling pathway in adipocytes as insulin itself. The effects observed are even better as insulin in its monomeric form is released predominantly from its supramolecular insulin assembly.

Example 17 describes histology and immunohistochemistry details of supramolecular insulin assembly of insulin. The diabetic rats treated with supramolecular insulin assembly were monitored for the presence of residual amount of supramolecular insulin assembly from the day of injection from one week to 12 weeks. Supramolecular insulin assembly deposits in subcutaneous as well as muscle tissues were detected using Congo red. Subcutaneous and muscle tissue sections were prepared, stained and analyzed as described in materials and methods. Tissues obtained after 24 h of supramolecular insulin assembly injection were found to bind with Congo red effectively, confirming the presence of higher amounts of supramolecular insulin assembly fibrils (FIG. 18). Congo red binding decreased in a time dependent manner and was negligible after 12 weeks (FIG. 18 a(i-x) &b(i-x)), confirming the release of insulin from the termini of supramolecular insulin assembly deposits. Same tissues were also checked for inflammation caused by supramolecular insulin assembly by H & E and immunostaining. Representative slides were subjected to H&E staining method and immunohistochemistry for the presence of inflammatory cells (FIG. 18 a(xi-xx) and 18 b(xi-xv).

As compared to the sections from LPS injected rats, where infiltration of proinflammatory cells were visible in both subcutaneous and muscle tissues stained with H &E (FIG. 19 a(i-ii)), supramolecular insulin assembly injected sections did not show any sign of inflammation even after 12 weeks (FIG. 18 a(xi-xv)). Similar results were observed in the case of immunostained slides where LPS from Escherichia coli was sufficient to attract huge number of proinflammatory cells after 72 h at the site of injection (FIG. 19 a(iii-iv)) whereas no such reaction was observed in animals treated with supramolecular insulin assembly (FIG. 18 a(xv-xx) and b(xi-xv)). These observations reinforce non-cytotoxic nature of the supramolecular insulin assembly being used. Amyloid formed at pH 2.0 binds congo red dye very efficiently as seen in FIG. 19 b, when injected subcutaneously. Moreover there is no decrease in the depot corroborating the data that no release of insulin monomers takes place from the fully formed amyloid (FIG. 19 b i-viii).

Example 18 describes alloxan model of diabetes. Male wistar rats were rendered diabetic using alloxan and their blood glucose levels were monitored. Administration of supramolecular insulin assembly II to diabetic rats, lowered the blood glucose level to near normoglycemic levels, and maintained a tight glycemic control for up to >120 days, in both pre-prandial and post-prandial conditions (FIG. 20 a&b). Serum insulin quantification was done using ELISA. From the day of injection, a sustained and constant release of human insulin is observed in the serum of the treated rats (0.5-0.9 ng/ml) (FIG. 20 c). Thus the physiologic effect seen by the lowering of the glucose levels in diabetic rat is due to the continuous release of insulin monomers from the SIA-II depot formed at the site of injection.

Example 19 Reduction of secondary complications related to hyperglycemia in type I diabetes: In type-1 diabetes, insufficient supply of insulin leads to increased protein degradation in skeletal muscles and lipolysis in adipocytes. Diabetic rats showed a marked decrease in skeletal muscle (˜20-40%) and abdominal fat (>60%) (Nathan, D. M., Cleary, P. A., Backlund, J. Y., et al. Intensive diabetes treatment and cardiovascular disease in patients with type 1 diabetes. N. Engl. J. Med. 353, 2643-53 (2005)). In contrast, supramolecular insulin assembly treated diabetic animals had normal weight for these tissues and were healthy. Development of cataract in diabetic rats as well as in insulin treated ones were observed (FIG. 21). While no cataract formation was observed in animals treated with SIA II, majority of untreated rats exhibited cataract as demonstrated in FIG. 21. Furthermore, the function of liver and kidney, the two main organs of the body which typically and severely get afflicted in diabetes were normal in supramolecular insulin assembly II treated rats as compared to their untreated or free insulin infused rats and is summarized in table 1.

Heart, kidney and liver sections were examined for the deposition of higher oligomers of SIA-II injected to diabetic rats after 12 weeks, visualized using congo red dye (FIG. 22). No deposition of oligomers was observed in any of the tissue sections.

Example 20 provides the details of detection of insulin degrading enzyme (IDE) and screening of antibodies against insulin. Subcutaneous resistance to insulin in Type-1 diabetes is a rare syndrome (Paulsen, E. P., Courtney, J. W. & Duckworth, W. C. Insulin resistance caused by massive degradation of subcutaneous insulin. Diabetes 28, 640-645 (1979) and Freidenberg, G. R., White, N., Cataland, S., O'Dorisio, T. M., Sotos, J. F. & Santiago, J. V. Diabetes responsive to intravenous but not subcutaneous insulin: effectiveness of aprotinin, N. Engl. J. Med. 305, 363-368 (1981)), defined as the lack of biological activity of subcutaneously injected insulin; nevertheless, efficacy for intravenously infused insulin is retained. This is mainly attributed to increased insulin degradation by IDE in the subcutaneous tissues. IDE degrades insulin specifically (Duckworth, W. C., Bennett, R. G. & Hamel, F. G. Insulin degradation: progress and potential, Endocr. Rev. 19, 608-624 (1998)) and the partially degraded insulin is reabsorbed into the circulation with increased immunogenicity but no biological activity. IDE is present in insulin responsive tissues and in insulin insensitive cells such as monocytes and lymphocytes. To check the development of such a resistance in supramolecular insulin assembly treated animals, biological activity of IDE and the presence of anti-insulin antibody were determined as described in methods section. IDE activity was negligible in all the serum samples (1-12 weeks) from supramolecular insulin assembly treated animals (FIG. 23). Similarly there was no presence of anti-insulin antibodies even after 12 weeks of treatment, supporting the absence of IDE activity (FIG. 24).

To see whether the insulin monomers released from supramolecular insulin assembly II had undergone any change in its structure or its binding dynamics, MTT assay on MCF 7 cell lines was performed. The proliferation of MCF 7 cells, when SIA was added to the culture was similar to that of those cells to which native insulin was added. Furthermore, the released monomers from the SIA II formed, also showed the same kinetics of cell proliferation. Insulin like growth factor I was used as a positive control for the proliferation of MCF 7 cells (FIG. 25). Insulin and IGF 1 have similar structure, and in the absence of the other, each can bind to the other receptor. But whereas IGF 1 is mitogenic, insulin upon binding to insulin receptor or IGF receptor does not cause proliferation of cells. Thus the monomers released from SIA II have the same binding kinetics as that of native insulin, and do not undergo any structural change.

Example 21 describes Streptozotocin model for induction of diabetes in mice. Dose response for human and bovine SIA in mice rendered diabetic using STZ. The administration of various dosage 20, 50, 100 and 200 μg of respective SIA to diabetic mice maintained the normo/near-normo glycemia for 5, 15, 30, 120 days respectively (FIG. 26 a-c).

Example 22 describes Streptozotocin model for induction of diabetes in rabbit. The administration of 1 mg/kg body weight of rH-insulin SIA-II to diabetic rabbit maintained the normo/near-normo glycemia for atlest 80 days (FIG. 27).

Example 23 provides details of the experiments carried out with supramolecular insulin assembly along with Exendin 4. For treatment of type II diabetes, supramolecular insulin assembly along with exendin 4 was administered as an adjunct therapy. The combination therapy administered was able to lower blood glucose levels and maintain at near normoglycemic levels in diabetic rats up to >30 days (FIG. 28). The levels of TAGs and FFA also remained near about normal as compared to only insulin or PBS treated rats, where the levels increased up to 1.5 fold in the serum as shown in Table 2.

The supramolecular insulin assembly formulation of the present invention shows surprising result of release of insulin monomers for a long period. Further, the supramolecular insulin assembly II of the present invention does not exhibit an abrupt large release of insulin; thwarting hypoglycemic stage in STZ treated diabetic rats. To validate the above unexpected result the intermediates of insulin supramolecular assembly II obtained during insulin fibrilization process at pH 7.0 was assessed. The intermediate supramolecular insulin assembly II is found to release insulin monomers at a constant rate for long duration. The intermediate (supramolecular insulin assembly II) selected does not show significant Congo-red binding indicating its failure to progress to an amyloid state and AFM analysis confirmed the presence of a linear association of elongated oligomers as the predominant species. The height of this unique entity is 18±5 nm compared to highly twisted fully grown fiber with height 12±5 nm suggesting that the elongated oligomers which form supramolecular insulin assembly are swollen and have retained native like structure. Similar non-fibrillar structures are also observed by TEM studies. The biological effectiveness of insulin is generally assessed by its ability to regulate glycemic level in the blood. The resultant decrease in the blood glucose concentration represents the most noticeable and, therapeutically, the most important effect of insulin. The efficiency of glycemic control in STZ-induced diabetic rats treated with single dose of supramolecular insulin assembly and compared with single-daily insulin injections was assessed. Both supramolecular insulin assembly treatment and insulin injection reduced the severity of hyperglycemia. Compared to insulin treatment, single dose of supramolecular insulin assembly of the present invention maintains near-normoglycemic levels (120 mg/dL) in the diabetic animal for a period of about 150-180 days.

The present invention further assesses the effect of supramolecular insulin assembly II therapy in regulation of blood glucose level. The supramolecular insulin assembly treated diabetic animals were subjected to overnight fasting. These fasted animals were able to maintain their fasting blood glucose levels within the normal range (60-100 mg/dl) and no pre-prandial hypoglycemia was observed. Taken together, these data provided that higher oligomeric state of supramolecular insulin assembly II compared to conventional insulin therapy achieves a tightly regulated glycemic control without fasting hypoglycemia in diabetic animals.

The present invention further assesses the effect of supramolecular insulin assembly II treatment on body weight. Intraperitoneal glucose tolerance test conducted to determine the onset of the action of supramolecular insulin assembly in case of severe hyperglycemia. The IPGTT blood glucose profile showed that both insulin and supramolecular insulin assembly treatment showed their effect within 30 min, suggesting no lag phase in release of bioactive insulin monomers from supramolecular insulin assembly II depot.

The present invention provides in vivo release profile of insulin from supramolecular insulin assembly by bovine/human insulin quantification in the serum using ELISA. In contrast to sigmoid release kinetics observed in vitro, in vivo release of insulin monomers from supramolecular insulin assembly followed zero order kinetics as expected for a sustained release. A sustained release of basal and above basal level (0.5-1.2 ng/ml) of insulin for maintaining normoglycemia was seen, which correlated well with the duration of the treatment. To validate the above release kinetics, radiolabeling of insulin with ¹²⁵I was done and ¹²⁵I labeled supramolecular insulin assembly were injected either subcutaneously or intramuscularly to STZ treated animals. The amount of insulin release was measured by monitoring CPM/ml. CPM/ml/μg (49912) was used for the quantification of insulin released in the serum at a particular time point and this paralleled to the amount of bovine insulin quantified using ELISA. After measuring counts, serum samples were resolved on Tricine-SDS-PAGE. The phosphor images developed showed bands corresponding to insulin monomer. The insulin monomers released from the supramolecular insulin assembly depot triggered efficaciously the insulin signaling cascade in insulin responsive adipocytes. Insulin released from the supramolecular insulin assembly in vitro and in vivo (serum), when added to isolated adipocytes was able to activate the intracellular mediators (i.e. PI3K, Akt, ERK1/2 and GSK3β) of the signaling pathway. Therefore, the insulin monomers released from supramolecular insulin assembly depot are biologically active and follow the same mechanism as insulin to regulate the glucose homeostasis in the body. The histochemistry also provides that the supramolecular insulin assembly II injected in animals formed a depot from which there is a slow and sustained release of bioactive insulin. Furthermore, there is no inflammation observed as opposed to infiltration of leucocytes in response to subcutaneously or intramuscularly injected LPS.

The present invention provides that the supramolecular insulin assembly therapy confers profound physiological benefits in diabetic animals. This is partially reflected in the significantly improved glycemic control as well as markedly reduced urea and creatinine concentrations due to improved liver and kidney functions in diabetic rats as provided in Table 1.

The present invention provides details of anti-insulin antibodies and insulin degrading enzyme (IDE) in serum on administration of supramolecular insulin assembly. The absence of anti-insulin antibodies even by the end of the 12^(th) week adds to the value of supramolecular insulin assembly as a treatment for diabetes mellitus. Its inability to elicit IDE in or around the site of injection is an important factor in prolonging the release of insulin from the supramolecular insulin assembly and the concomitant beneficial anti-diabetic affect.

The present invention provides that insulin monomer released from supramolecular insulin assembly II has equivalent biological function as soluble insulin. A significant difference lies in the duration of action, whereas it is only the 6-10 hrs for standard insulin injection, but surprisingly so, about 10 days to about 180 days or more depending on the dosage of the supramolecular insulin assembly II. This may be attributed to the remarkable stability of insulin in the supramolecular insulin assembly, which forms a depot at the site of injection for the supply of the most physiologically relevant form of insulin, viz. insulin monomers, for long periods of time.

Administration of supramolecular assembly II of human insulin led to an even better glycemic control, observed over a period of 135-180 days. Both subcutaneous and intramuscular injection of the insulin oligomer resulted in near normoglycemia as evident from the figure.

Released insulin in serum was quantified using ELISA and was observed to maintain an almost constant level, resulting from a slow and sustained release from the depot.

Male wistar rats rendered diabetic with alloxan and streptozotocin treated diabetic C57b1/6 mice (served as another model of diabetes), both showed near normoglycemic blood glucose level upon being treated with supramolecular insulin assembly II.

The western blot data obtained for human supramolecular assembly II insulin is essentially the same, showing the activation of the signaling pathway by the released insulin monomers.

The supramolecular insulin assembly I is characterized by swollen and more globular species with 18±2 nm height. The unfolding of the peptide structure during the process of amyloid formation results in globular monomeric species randomly distributed over the surface individually. Further onwards there is a linear association of these monomers at stage II of the human insulin supramolecular assembly II, albeit retaining their swollen morphology. The oligomers formed represent elongated clusters, same as bovine insulin with a height of 18±4 nm. In case of supramolecular insulin assembly III (closer to the fibril stage succeeding SIA II), an increase in density of higher oligomeric structures is seen. The structure is more compact with a height of 5±1 nm. The overall structural morphology resembles bovine SIA stages, with fully formed fibers seen further onwards.

The present invention provides the efficacy as well as the feasibility of supramolecular insulin assembly therapy for the significant improvement of blood glucose level without causing fasting hypoglycemia in STZ-induced diabetic animal model. Unlike intensive insulin therapy, by which blood glucose levels is controlled by an increased frequency of insulin injection with concomitant risk of hypoglycemia, the significantly improved glycemic control using supramolecular insulin assembly therapy, is accomplished without the need for multiple insulin injections and without excessive body weight gain.

A further value to this innovation is added by the extension of these studies to those ailments requiring a sustained and continuous infusion of insulin as a therapy, as in the case of Diabetes Mellitus type II (DM II). Both Exendin 4 and insulin, in combination is utilized as a potent therapy for DM II. Exendin 4 is known to lower blood glucose levels, through decrease in the absorption of food from the stomach. It also delays gastric emptying, lowers the levels of HbAc and prevents the large increase in weight observed due to insulin therapy. An amyloidogenic tag of GNNQQNY was attached to the C-terminal of Exendin 4, to promote its aggregation into an oligomeric complex, from which the native monomers of Exendin 4 is released as is the case with insulin reported in the above section. Exendin 4a is used as an adjunct therapy along with SIA I and II for the treatment of DM II in animal subjects.

The present invention also provides the usage of supramolecular assembly of calcitonin as a potential therapeutic candidate for the treatment of osteoporosis in ovariectomised rats. Details are provided in Example 24. Supramolecular calcitonin assembly or SCA is incorporated into Alzet pumps, from where there is a slow and continuous release of calcitonin into the blood. This slow release of calcitonin alleviates the symptoms of osteoporosis, maintaining normal body weight and serum calcium and phosphorous levels.

A solution of Salmon calcitonin-1 and 2 mg/ml was prepared in PBS and incubated at 37° C. for 80 hrs. The kinetics of calcitonin amyloid fibril formation was monitored by measuring turbidity at 400 nm at different time interval. As shown in FIG. 29 the rate of fibril formation is concentration dependent and almost completed after 44 h. The SCA-I, SCA-II and SCA-III were formed at 6, 8 and 12 h, respectively.

The release of free calcitonin from the SCA was monitored in 2% mannitol in a constant volume of 1 ml and by dialyzing through a dialysis membrane. The release was monitored by absorbance at 275 nm. As shown in FIG. 30, the release of calcitonin from SCA in a constant volume of 1 ml follows a bell shaped curve like that of supramolecular insulin assembly. However, continuous release was observed under dialysis through a membrane and was similar to insulin release from SIA. The release of calcitonin from fully grown calcitonin fibers was very slow and could be considered negligible for further experiments. The calcitonin SCA was further used for the in vivo experiments for the treatment of osteoporosis in ovariectomized rat.

As mentioned in experimental section, five groups of rats (10 rats in each group) were given different treatment. The body weight and serum profile of calcium, phosphorous and calcitonin was monitored. The release kinetics of salmon calcitonin from SCA in ovariectomized rats treated with SCA in Alzet and endogenous rat calcitonin in control rats was determined and is shown in FIG. 31. Calcitonin level was maintained at a relatively higher level in rats treated with SCA, compared to that of other groups. This shows that the calcitonin SCA solution in Alzet pump releases calcitonin in the biologically active form with a constant and slow rate, which in turn treated the symptoms of osteoporosis in OVX rat for up to 60 days compared to daily treatment with soluble calcitonin.

The final body weight for the four groups of rats was monitored. Rats from all four groups gained weight during the course of the study. The vehicle-treated OVX rats weighed approximately 11% more than vehicle-treated control rats at the end of the 8 week study (328±19 g vs. 296±09 g, p<0.05). The mean body weight of OVX rats treated with CT intermittently or continuously with SCA were significantly decreased compared with that of vehicle-treated OVX rats.

Serum biochemical data are listed in Table 3. The serum CT concentration was measured in all groups during and at the end of 8 week in OVX rats treated with SCA and was significantly higher than that of vehicle-treated OVX, but not than that of control rats. Mean serum calcium levels in OVX rats treated with SCA was significantly lower than that of all other groups. Mean serum phosphorus level was also significantly increased in vehicle-treated OVX rats relative to vehicle-treated control rats. In contrast, treatment of OVX rats with CT either intermittently or continuously in case of SCA, significantly decreased serum phosphorus concentration compared to that of vehicle treatment to OVX rats. Furthermore, this variability in OVX rats treated with SCA was significantly lower than that in OVX rats treated with CT intermittently.

Screening the antibody against salmon calcitonin in all the groups showed negligible antibody in Case of control, vehicle treated and calcitonin SCA treated rats. However, lower level of antibody raised against salmon calcitonin in calcitonin treated group (intermittently or continuously).

The present invention also provides the usage of supramolecular ibuprofen tagged peptide assembly as a potential therapeutic candidate for the treatment of arthritis and arthritic pain. Details are provided in Example 25.

Arthritis is a very important clinical condition and a common disabling ailment especially of middle and old age. Non-steroidal anti-inflammatory drugs (NSAIDs) are widely used to treat pain, fever, and inflammatory conditions including Osteoarthritis. The current therapy for this disorder is unsatisfactory, and the common drugs used have many toxic side-effects and are mostly palliative. Carrageenan induced arthritis produces acute inflammation, which is suppressed by corticosteroids as well as vasoconstrictors. Knee joint arthritis was produced using the KC model of arthritis, by injecting kaolin and carrageenan into the synovial cavity of the knee. Male Wistar rats were grouped into five groups, and arthritis was induced in four of the groups using kaolin/carrageenan (KC). PBS was injected into the control group. After half an hour, various dosages of Ibuprofen (10 ang 50 mg/kg b wt), and Ibuprofen-TTR was administered orally and intraperitoneally respectively. The rats were placed on the hot plate analgesiometer after an hour, and their latency in licking their paw was monitored. Control rats, injected PBS, responded to the heat in about 6-7 sec by licking their paw (FIG. 32 a). KC injected rats were extremely sensitive and could not bear the heat for more than 3-5 sec. In comparison, those rats which were given Ibuprofen orally were able to endure heat up to 12 sec for 10 mg/kg b.wt and 17 sec for 50 mg/kg b.wt of Ibuprofen. The latency time period was about 15 sec for those rats administered supramolecular Ibuprofen-TTR assembly i.p. The slow and continuous release of Ibuprofen from the supramolecular assembly is even more evident, when on consecutive days, the rats still show about 12-16 sec of latency in licking their paw, without a second administration of the drug (FIG. 32 b), whereas, Ibuprofen had to be injected daily for observing its effect on the rats. The effect of the supramolecular Ibuprofen-TTR assembly lasts up to 3-4 days, as indicated by the sharp decrease in the latency time (FIG. 32 b)

Inflammation caused by the injection of carrageenan into the rat paw causes edema to develop. Thus measurement of increase in rat paw volume is an effective method to monitor inflammation caused during arthritis. Control and treated rat paw volume was measured using a hydroplethysmometer, by subtracting the basal volume of paw before injection of KC. A sharp increase is seen in case of carrageenan control treated with PBS, rat paw volume almost increasing by 0.8-0.92 ml (FIG. 33). The increase in paw volume was comparatively less (0.4 ml) for those rats treated with supramolecular Ibuprofen-TTR assembly, and started increasing only on the fourth day, indicating a consumption of the depot with release of the drug-Ibuprofen. Whereas for groupie and III, Ibuprofen had to be injected daily, to prevent the sharp increases in rat paw volume, with 50 mg/kg b.wt being more effective. The data demonstrate the effectiveness of supramolecular Ibuprofen-TTR assembly in alleviating the symptoms of arthritis for up to 3-4 days with only a single injection of the complex.

Thus the present invention not only encompasses metabolic disease such as Diabetes, both type I and II, but can be further extended to all those diseases such as chronic pain, sepsis, arthritis, osteoporosis, inflammation, etc, where a continuous infusion of the therapeutic drug is required, be it a peptide, protein or a small drug molecule. This invention also discusses the feasibility of using insulin oligomer (SIA I, SIA II and SIA III) for the treatment of DM I, DM II and borderline diabetic cases. This methodology of utilizing the oligomers of the drug as a depot for treatment can be extended to many more diseases, having a all round, broad spectrum applicability.

The following examples are given by the way of illustration of the invention contained in the present invention and therefore should not be construed to limit the scope of the present invention.

EXAMPLES

It should be understood that the following examples described herein are for illustrative purposes only and that various modifications or changes in light of the specification will be suggestive to person skilled in the art and are to be included within the spirit and purview of this application and the scope of the appended claims.

Example 1 Insulin Fibrilization

Bovine and rH insulin, 2 mg/ml, was dissolved in phosphate buffer saline (50 mM, pH 7.0) or pH 2.0 (Hydrochloric acid in water) and incubated at 37° C. for 72 hr-7 days with constant agitation at 180 rpm. The kinetics of fibril formation was monitored by monitoring the acquisition of fluorescence by Thioflavin T (ThT).

Example 2 Thioflavin T Fluorescence

Th-T fluorescence was measured on a Jobin Yvon Fluoromax spectrofluorometer using slit widths of 3 nm and 5 nm for excitation and emission respectively. Samples incubated with 50 μM of Th-T for 15 minutes were excited at 450 nm and their emission was monitored in the range of 460-560 nm. The data was corrected for blank and inner filter effect using the following equation, Fc=F antilog[(A_(ex)+A_(em))/2]

Where Fc is the corrected fluorescence and F is the measured one, A_(ex) and A_(em) are the absorbance of the reaction solution at the excitation and emission wavelengths respectively.

Kinetics of formation of fibrils by bovine and rH insulin at 37° C. is provided in FIG. 1. FIG. 1 (a) demonstrates kinetics of fibril formation at pH 7.0 monitored with 50 μM Th-T fluorescence.

Example 3 In vitro Monomer Release Kinetics of Intermediates and Fully Formed Fibrils Formed at pH 2.0 and 7.0

200 μl (equal to 400 μg of insulin) aliquots were withdrawn at different time point from the insulin fibrilization reaction at pH 2.0 and 7.0, 37° C. The supramolecular insulin assembly intermediate produced were isolated by centrifugation. The pellet obtained was washed with PBS and resuspended in 1 ml PBS in an eppendorf. The cap of the eppendorf containing the intermediates was removed and the eppendorf was sealed with 12 kDa cut off dialysis membrane. The eppendorf was then inserted through its membrane side into a 50 ml Falcon tube containing 20 ml PBS with 0.02% sodium azide and the kinetics of the release of insulin was monitored for 15 days under constant stirring. The kinetics of release was monitored spectrophotometrically at 280 nm and by its intrinsic (tyrosine) fluorescence. The amount of insulin released per hour was calculated. FIG. 2 a provides in vitro release of insulin from Supramolecular insulin assembly II intermediate monitored by absorbance at 280 nm and intrinsic tyrosine fluorescence. The Th-T intensity of solution inside the dialysis membrane at Oh and 15 days is also given.

To study release profile of different intermediates small aliquots of intermediates and fully formed amyloid fibrils at both pH 2.0 and 7.0, 37° C. were withdrawn from the fibrilizaton process at regular intervals and centrifuged at 10,000 rpm for 10 minutes. Supernatant was removed and after washing the pellet twice with PBS, resuspended in fresh PBS. The release of monomeric insulin was monitored spectrophotometrically at 280 nm, 37° C. Release kinetics was studied in two different conditions. In one, the pellet was suspended in PBS and dialyzed through a 12 kDa cut off membrane in 20 ml PBS with constant stirring (FIG. 2 a-c). In second, the pellet obtained was suspended in 1 ml of PBS and the absorbance of the supernatant was read at 280 nm (FIG. 2 d).

Example 4 Congo Red Binding

The amount of Congo red bound to the insulin oligomers/amyloid was estimated as reported earlier (Klunk, W. E., Jacob, R. F. & Mason, R. P. Quantifying amyloid by Congo red spectral shift assay. Methods Enzymol 309, 285-305 (1999)) using the equation, moles of Congo red bound/L of amyloid suspension=A₅₄₀ nm/25295−A₄₇₇ nm/46306.

FIG. 3 provides congo-Red binding studies with native insulin, supramolecular insulin assembly II, supramolecular insulin assembly III and amyloid insulin.

Example 5 Tyrosine Fluorescence

The dialysate of supramolecular insulin assembly withdrawn at different time intervals in a 0.2 ml quartz cuvette was excited at 270 nm and emission recorded between 320 to 370 nm. Slit width of 5 nm was used for both excitation and emission. FIG. 2( a) provides in vitro release of insulin from supramolecular insulin assembly II intermediate monitored by absorbance at 280 nm and intrinsic tyrosine fluorescence. The Th-T intensity of solution inside the dialysis membrane at Oh and 15 days is also shown.

Example 6 Fourier Transform Infrared Spectroscopy (FTIR)

IR spectra were recorded with a Bruker Tensor 27 bench top FTIR spectrometer, equipped with a liquid N₂-cooled mercury cadmium telluride detector. Insulin samples were analysed on Bio-ATR and 256 interferograms were recorded at room temperature with a resolution of 2 cm⁼¹. For each spectrum, water vapor was subtracted and baseline corrected.

SIA I, II and III were also characterized using ATR-FTIR. Distinct spectra corresponding to each stage was observed (FIG. 1 d).

Supramolecular insulin assembly I, II and III of bovine and rH insulin were also characterized using ATR-FTIR. Distinct spectra corresponding to each stage was observed (FIG. 4). A shift of the IR band towards lower frequencies is observed during fibrillization. Supramolecular insulin assembly II (SIA-II) has a sharp peak at 1647 cm⁻¹ and 1645 cm⁻¹ for bovine and rH insulin respectively, while the fully formed amyloid peaks at 1630 cm⁻¹ and 1628 cm⁻¹ for the same. The FTIR spectra is in good agreement with the CR binding data showing that the conformation of SIA-II is still largely helical, albeit with an increase in the content of random coil structure

Example 7 Atomic Force Microscopy (AFM)

Pico plus atomic force microscope (Agilent Technologies) was used in magnetic acoustic MAC (contact) mode for imaging. Images were recorded in air with either a bare mica surface or mica with sample using MAC cantilever Type II (spring constant of cantilever: 2.8 N/m, Frequency: 59.722 kHz). Samples were withdrawn from the fibrilization reaction mixture at various time points, diluted 20 fold with water and immobilized on freshly cleaved mica for 2 minutes. The samples were washed with nanopure water, dried under N₂ and subjected to AFM analysis.

FIG. 5 provides morphologies of supramolecular insulin assembly intermediates and insulin fibrils studied by Atomic Force Microscopy. FIG. 5( a) insulin monomer (b) Supramolecular insulin assembly-I intermediate, pH 7.0, (c) Supramolecular insulin assembly II, pH 7.0, (d) Supramolecular insulin assembly intermediate III, pH 7.0, (e) human SIA I, (f) human SIA II, (g) human SIA III, and (h) Fully formed fibrils at pH 7.0., (i) provide supramolecular insulin assembly intermediate formed at 6 hrs, pH 2.0 at 37° C., (j) provides fully formed amyloid fibril formed at pH 2.0.

Example 8 Transmission Electron Microscopy (TEM)

For TEM studies, samples were vortexed and immediately absorbed to fomber-coated 300 mesh copper grids as such or diluted to 1:2-20 fold with mili-Q water and washed with deionized water. Grids were incubated in 3% Uranyl Acetate for 2-5 min and dried under infra red light for examining the samples by negative stain. The grids were visualized with a Phillips CM-10 at 80 kV. The pictures were captured using MegaView III camera and analyzed using the Imaging Software from Imaging System Phillips. FIG. 6 provides negative staining TEM micrographs of insulin fibrils and supramolecular insulin assembly intermediates, wherein FIG. 6( a) provides supramolecular insulin assembly I intermediate, pH 7.0, FIG. 6( b) provides supramolecular insulin assembly II, pH 7.0, FIG. 6( c) provides supramolecular insulin assembly intermediate III, pH 7.0, FIG. 6( d) provides mature fibers at pH 7.0, FIG. 6( e) provides fiber formed at pH 2.0, 37° C.

Example 9 Rat Model of Diabetes

Nine weeks old Male Wistar rats (Rattus norvegicus albinus, Rodentia mammalia) weighing 210±10 g were used. Rats were housed in commercially available polypropylene cages and maintained under controlled temperature conditions on a 12 h light-dark cycle and allowed to access food and water ad libitum.

Streptozotocin Model for Induction of Diabetes in Rats

Male Wistar Rats weighing 250-300 g were divided into four groups and blood glucose estimation was done using Roche Accu Check glucose strips. Rats were kept on fasting for 48 hours. 50 mg/kg b.wt of Streptozotocin prepared freshly in citrate buffer (pH 4.5) was administered intraperitoneally to 10-20 rats. Food was provided immediately and blood glucose levels were checked after three days. The animals were grouped according to their blood glucose level (group I: 250-350 mg/dl, group II: 350-450 mg/dl and group III: >450 mg/dL). High blood glucose levels were maintained for a week with 2-6 U/kg body weight (b.wt) of bovine insulin. All STZ-treated rats developed hyperglycemia (blood glucose levels>250 mg/di), 5 days after STZ injection, and their serum insulin levels were quantified using rat insulin solid enzyme-linked immunosorbent assay (ELISA) (Mercodia). Rats with >250 mg/dL of glucose and negligible (˜0.08 ng/ml) serum insulin levels were considered diabetic and used for the experiment.

Example 10 Supramolecular Insulin Assembly Treatment

After one week of maintaining high blood glucose levels with insulin, the rats were divided into three groups, each containing 5 rats. Group I rats were administered single dose of 4 U/kg b.wt of bovine insulin intraperitoneally per day. Group II rats were injected 4 U/kg b.wt of insulin twice daily. Group III treated with 200 μg of supramolecular insulin assembly II (subcutaneously as well as intramuscularly) in 100 μl of PBS and group IV rats were administered 100 μl of PBS, constituting the diabetic control. A group of 5 normal rats injected 100 μl of PBS, served as the non-diabetic control. Body weight and blood glucose levels, both pre-prandial after 8-10 hr fasting and post-prandial were checked initially daily and then with decreasing frequency. FIG. 7 shows in vivo efficacy of supramolecular insulin assembly (alternatively pre-amyloid insulin) in glucose homeostasis. (a) Blood glucose level in response to various dosages of supramolecular insulin assembly-II (bovine) administered both subcutaneously and intramuscularly. (b) Blood glucose level in response to various dosages of supramolecular insulin assembly-II (r-human) administered both subcutaneously and intramuscularly.

FIG. 8 shows Post-prandial blood glucose levels monitored over a period of 135 days after administration of bovine SIA-II (a) Bovine insulin, (b) rH insulin. FIG. 9 shows Pre-prandial blood glucose levels monitored over a period of 160 days after administration of human SIA-II (a) Bovine insulin, (b) rH insulin. FIG. 10 shows blood glucose level monitored after administration of insulin amyloid formed at pH 2.0 and 7.0. FIG. 11 shows body weight profile of SIA-II treated diabetic rats, diabetic control and non-diabetic control rats.

Example 11 Intraperitoneal Glucose Tolerance Test (IPGTT)

The STZ treated (n=12) and normal rats (n=4) were kept on fasting for 12 hrs. Blood glucose levels were monitored as described above. For glucose tolerance test was done. Briefly, animals were infused with 3 g/kg body weight of glucose, intraperitonealy, followed by injection of 4 U/kg b.wt of Bovine insulin to group 1,100 μl of amyloid insulin to group II and 100 μl of PBS (vehicle) to group III rats. Blood glucose levels were monitored at 0, 30, 90, 150, 270 and 330 min after treatment. Serum was isolated for various time points and a graph was plotted between blood glucose level and time. FIG. 12 provides blood glucose profile of Intraperitoneal Glucose Tolerance Test (IPGTT).

Example 12 Serum Insulin Quantification

Serum was isolated from the blood samples collected and stored at −20° C. till further analysis. Bovine and rat insulin levels were quantified using solid phase two site enzyme immunoassay (ELISA) from Mercodia (Sweden), by following the manufacturer's protocol. FIG. 13 a provides quantification of serum human and bovine insulin using ELISA in STZ treated rats in response to supramolecular insulin assembly injected SC or IM, FIG. 13( b) provides quantification of serum bovine insulin of IPGTT, FIG. 13( c) provides serum rat insulin ELISA performed for IPGTT.

Example 13 I¹²⁵ Labelling of Insulin

To further validate and quantitate the in vitro release from the termini of insulin SIA II, labeling of insulin with ¹²⁵I was done (Pause, E., Bormer, O. & Nustad, K. Radioiodination of proteins with the iodogen method, in RIA and related procedures in medicine, international atomic agency, Vienna, 161-171 (1982)). Supramolecular insulin assembly formed from labeled insulin had a specific activity of 49912 CPM/ml/μg. 50 μl of supramolecular insulin assembly (4991200 CPM) was injected either subcutaneously or intramuscularly and blood glucose levels were monitored and serum samples were collected at 0, 30 min, 1 h, 4 h, 10 h, 24 hrs, thereafter once a day, and then on alternate days or once in a week. Counts in per ml of serum were measured (FIG. 14 a). As shown in FIG. 14 b, blood glucose profile was same as observed with the unlabeled SIA II. The CPM/ml calculated remained almost constant (FIG. 14 a) when plotted against the number of days of treatment. However, there was an initial high count at 30 min-4 hrs, which then gradually decreased to a constant level of 2000-3000 in 10 hrs. The amount of insulin released in blood was calculated and was in the range of 0.5-1.2 ng/ml which corresponded to the basal or slightly above basal level of insulin in the serum as observed with ELISA (FIG. 14 b). To further prove that the released insulin from supramolecular insulin assembly is monomeric, serum of different time points were resolved on tricine-SDS-PAGE (Schaogger, H. & Von Jagow, G. Tricine-sodium dodecyl sulfate-polyacrylamide gel electrophoresis for the separation of proteins in the range from 1 to 100 kDa. Anal Biochem 166, 368-379 (1987)) and radiogram was developed using the phosphor imager. As shown in FIG. 15, the band in serum corresponds to free insulin monomer and its intensity remained constant for a long period when equal amount of serum was loaded. A decrease in intensity was observed after 20 days showing usage and depletion of the supramolecular insulin assembly depot over a period of time together with some effect of the decay of the radio-label itself.

Example 14 Hyperglycemic Clamp After Treatment with Supramolecular Insulin Assembly II

Male wistar rats were anesthetized (Isoflurane 2%) and a carotid and jugular catheter installed to allow blood withdrawal and glucose injections (20% glucose solution) to clamp blood glucose level at 600 mg/dL. Following a 12 hours fasting period, glucose was infused in all groups to make them hyperglycemic. This was followed by blood withdrawal at indicated time intervals, for blood glucose measurements and the rate of glucose infusion to retain them hyperglycemic were calculated. This procedure was repeated after one and three months of SIA II administration (FIG. 16 a-c).

Example 15 Isolation and Primary Culture of Rat Adipocytes

Rat adipocytes were isolated and cultured according to the method described by Björntorp et al. (Björntorp, P., Karlsson, M., Pettersson, P. & Sypniewska, G. Differentiation and function of rat adipocyte precursor cells in primary culture. J. Lipid Res. 21, 714-723 (1987)). Male Wistar rats fed freely were sacrificed and epididymal fat tissue was dissected and collected in reagent A (HBSS, 100 U/ml penicillin, 100 μg/ml streptomycin and 50₁1 g/L gentamycin). The tissue was washed properly in HBSS. Following this the tissue was cut and minced finely and transferred to a falcon, centrifuged at 200 g for 2 min. The layer of transparent oil was removed and the adipocyte cell layer (thick and dense) was added to three times the volume of reagent B (reagent A containing 0.1% BSA and 1 mg/ml Collagenase) in a flask. The flask was incubated at 37° C. for 60 min with continuous slow shaking. The reaction was stopped by addition of DMEM complete media (with HEPES 15 mM, glc, 0.1% BSA, 50 nM adenosine and 1% fetal bovine serum) three times the volume and incubated at room temperature for 5 min. The reaction was transferred to a falcon and centrifuged at 200 g for 10 min. Adipocytes were collected after discarding the top layer of oil and washed twice with reagent A by centrifuging at 200 g for 10 min. Cells were dispensed into a flask with appropriate volume of DMEM complete media and incubated for 24 hrs at 37° C. For insulin signaling, adipocytes were centrifuged and maintained in serum free medium for 12 hrs before plating approximately 2 ml into 6 well culture plates, and incubated further for 2 hrs.

Example 16 Western Blot Analysis of Total Cellular Lysates

Plated cell were incubated with either 20 nM insulin, 50 μl of supramolecular insulin assembly and in vitro released insulin (monomers) or 50 μl of serum from rats treated with insulin, supramolecular insulin assembly and PBS for 10 min. After incubation, the cells were collected in a falcon tube and centrifuged at 200 g for 10 min. The top layer of adipocytes were collected in an eppendorf and kept in ice. 500 μl of lysis buffer (20 mM Tris pH 8.0, 1% NP 40, 137 mM NaCl, 1 mM MgCl₂, 1 mM CaCl₂, 1 mM DTT, 10% glycerol, 1 mM PMSF, 0.4 mM sodium orthovanadate and protease inhibitor cocktail) was added and the samples were frozen at −80° C., for 2 hrs. This was followed by thawing and incubating at 4° C. for 4 hrs with constant rotation. The supernatant was collected after centrifugation at 13000 rpm for 30 min and protein concentration in cell lysate was estimated using Bradford reagent. Fifty micrograms of total cellular protein were applied to each lane and were separated on 10% SDS-PAGE and transferred to nitrocellulose membrane using Bio-rad wet transfer apparatus at 4° C. overnight. After transfer, the blot was removed and stained with Ponceau-S for the visualization of transferred bands, and destained further with water. The membrane was blocked for 1 hr at 37° C. with 5% skimmed milk in PBS, pH 7.4, washed and then incubated overnight in primary antibody (1:1000 dilution using 1% skimmed milk in PBS) of PI3K, p-Akt, total Akt, p-Gsk3β, Gsk3β, ERK1/2, GAPDH and 13 actin (antibodies from cell signaling) at 4° C. After washing with PBST, the blot was incubated for 1 hr in respective secondary antibody (HRP-conjugated), and immunoreactive bands were visualized using the ECL western blotting protocol (Amersham). FIG. 17 provides western blot (WB) analysis of cultured adipocytes for insulin signaling cascade. Adipocytes treated with (a) PBS, insulin, SIA-II, insulin released from SIA-II, (b) serum as indicated, and analysed for insulin signaling.

Example 17 Histology and Immunohistochemistry

Rats were injected 200 μg of insulin SIA-II or 150 μg of Lipopolysaccharides (LPS) from Escherichia coli (Sigma-Aldrich, MO, USA) either through intramuscular or subcutaneous injections into thigh muscle and dorsal skin respectively. LPS injected rats were sacrificed after 48 h of injection whereas rats injected insulin SIA-II were monitored from 1 to 12 week and tissue sections were excised at an interval of every 7 days. Rats were anesthetized by ketamine and perfused with 4% paraformaldehyde. Skin and thigh muscles were removed and the injection site was excised out. Tissues were then processed for paraffin embedding and were sagitally sectioned at a thickness of 10 μm and further processed for routine hematoxylin-eosin (H & E) staining to see histology and the infiltration of inflammatory cells, Congo red staining (Lee, G. & Luna, H. T. Manual of Histologic staining methods of armed forces institute of pathology. 3rd Ed. McRaw-Hill book company (1960)) for the presence of residual SIA-II and Immunohistochemistry (Sanz M J, Marinova-Mutafchiev L, Green P, Lobb R R, & Feldmann M, Nourshargh S. IL-4-induced eosinophil accumulation in rat skin is dependent on endogenous TNF-alpha and alpha 4 integrinNCAM-1 adhesion pathways. J Immunol. 160, 5637-5645 (1998)) with antibodies against CD11b, RT-1A, and CD6 (BD Pharmigen, CA, USA). All immunoflorescent slides were mounted permanently with antifade reagent+mounting medium (Molecular probes, Eugene, Oreg., USA) and observed under florescent light for FITC conjugated antibodies. CR and H&E stained slides were mounted with citramount medium (Polysciences, PA, USA). H&E sections were observed under bright light whereas, CR stained slides under bright and polarized lights (Nikon Eclipse 80i, Nikon, Japan). Images were captured using DS SMc CCD camera (Nikon, Japan) and were analyzed by NIS-Element software (Nikon, Japan).

Example 18 Alloxan Model for Induction of Diabetes in Rats

Male Wistar Rats weighing 250-300 g were divided into four groups and blood glucose estimation was done using Roche Accu Check glucose strips. Rats were kept on fasting for 24 hours. 150 mg/kg b.wt of Alloxan prepared freshly in citrate buffer (pH 4.5) was administered intraperitoneally to 10-20 rats. Food was provided immediately and blood glucose levels were checked after three days. The animals were grouped according to their blood glucose level (group I: 250-350 mg/dl, group II: 350-450 mg/dl and group III: >450 mg/dL). High blood glucose levels were maintained for a week with 2-6 U/kg body weight (b.wt) of bovine insulin. 60% of Alloxan-treated rats developed hyperglycemia (blood glucose levels>250 mg/dl), 5 days after injection, and their serum insulin levels were quantified using rat insulin solid enzyme-linked immunosorbent assay (ELISA) (Mercodia). Rats with >250 mg/dL of glucose and negligible (˜0.18 ng/ml) serum insulin levels were considered diabetic and used for the experiment.

Example 19 Examples of Clinical Parameters Examined

Biochemical assays were performed for the evaluation of toxicity of supramolecular insulin assembly treatment. Serum glutamate oxalo-acetate transaminase (SGOT), serum glutamate pyruvate transaminase (SGPT), total Bilirubin, Bilirubin, Alkaline Phosphatase, Serum total proteins, Serum Albumin, Serum Globulin, Serum A/G ratio, Kidney function test (KFT), Cataract Formation, Adipose Tissue weight, Body Weight and Appearance were estimated using assay kits available from Merck India Ltd. Table 1 provides the analysis of clinical parameters for the evaluation of toxicity of Insulin SIA II. Serum isolated from blood samples collected at the end of the three month study and subjected to various tests indicated in the Table. Results are mean±s.d. of three different experiments having n=4 animals in each group.

Example 20 Detection of Anti-Insulin Antibodies and Insulin Degrading Enzyme (IDE) in Serum

Indirect ELISA was performed for the detection of anti-insulin antibodies in the rat serum by following the standard ELISA protocol. Indirect ELISA was performed for the detection of anti-insulin antibodies in the rat serum by following the standard ELISA protocol. Briefly, 200 μl of 2 mg/ml of bovine insulin in 50 mM carbonate buffer, pH 9.6, was coated onto a 96 well ELISA plate and kept overnight at 4° C. 5% BSA in PBS was used for blocking at 37° C. for 1 hr. The plate was then washed with PBST (0.02% Tween 20) and 20031 of 1:100 diluted serum was added and kept at 37° C. for 1 hr. Further rounds of washing with PBST was followed by the addition of 1:10000 diluted anti-rat IgG-HRP conjugated 2° antibody and incubated for 2 hrs, 37° C. Color was developed using TMB as a substrate and reaction stopped by the addition of conc H₂SO₄. The plate was read at 450 nm spectrophotometrically. Anti-insulin antibody was used as a positive control for the reaction. IDE was quantified from the serum using Insulysin/IDE InnoZyme™ Immunocapture Activity Assay Kit (Calbiochem) following the manufacturer's protocol. Rat IDE provided in the kit served as the positive control.

Cell Proliferation Assays:

Cells were plated in 24-well plates with 10,000 cells/well in regular DMEM media containing 10% FBS. Cells were switched to Serum Free Media for 12 h and then treated as indicated in the figure legends. All treatments were done in triplicates. Growth was measured 3 days after treatment. Growth was assayed by the MTT assay. A total of 50 μl of 5 mg/ml MTT solution in PBS was added to each well. After incubation for 4 h at 37° C., formazan crystals were lysed with 500 μl of solubilization solution (20% SDS, 50% DMSO). Absorbance was measured with a plate reader at 570 nm using a 670-nm differential filter.

Example 21 Streptozotocin Model for Induction of Diabetes in Mice

Inbred 12-16-week-old C57BL/6 male mice were used. Mice were injected intraperitoneally with 50 mg/kg b.wt of streptozotocin daily for 5 days. Blood glucose levels were estimated after two weeks. Mice with >300 mg/dl of blood glucose were considered diabetic and selected for further experiments. A total of six groups were made, with each group consisting of six mice each. Various dosages, such as 10 μl, 25 μl, 50 μl and 100 μl of bovine/human insulin SIA-II was administered either subcutaneously or intramuscularly to mice rendered diabetic using Streptozotocin, with the two other groups serving as the diabetic and the non-diabetic group. Both fasting and fed blood glucose levels were monitore using the Roche Accu Check glucose strips.

Example 22 Streptozotocin Model for Induction of Diabetes in Rabbit

Male New Zealand rabbits, weighing between 1000 and 1200 g were used. Animals were maintained under controlled conditions of humidity, temperature (22±2° C.) and 12 h light and dark cycle. The experimental protocol and animal handling was in accordance with the Institutional animal ethics committee of the National Institute of Immunology, New Delhi, India. For induction of experimental diabetes, rabbits used were fasted for 12 h, followed by administration of 80 mg/kg b.wt of Streptozotocin, prepared in citrate buffer, pH 4.5. Blood glucose levels were checked after three days.

Rabbits showing BGL>450 mg/dL were termed diabetic and further divided three groups of three rabbits each. Group I—normal healthy rabbits, group II—diabetic treated with insulin, group III—diabetic treated with SIA-II (SC) and group IV—diabetic treated with PBS.

Example 23 Model for Induction of Diabetes Type II in Wistar Rats and its Treatment Using SIA

Male Wistar rats, 7 weeks of age, and weighing approximately 200 g, were used for all studies. Animals were fed either a normal chow diet consisting (as a percentage of total kcal) of 12% fat, 60% carbohydrate, and 28% protein or a high-fat diet consisting of 40% fat, 41% carbohydrate, and 18% protein. After 2 weeks on either diet, animals (with the exception of non-injected controls) after an overnight fast were injected with STZ (50 mg/kg) into the tail vein via a temporary indwelling 24-gauge catheter. Animals had free access to food and water after the STZ injection, and both STZ-injected and non-injected animals were continued on their original diets (chow or fat) for the duration of the study. Animals with high blood glucose levels were administered either PBS as vehicle, insulin SIA, or insulin SIA with Exendin 4a subcutaneously. Blood was collected and serum was separated by centrifugation and analyzed for concentrations of glucose (glucose strips, Accucheck, Roche), insulin (Insulin Elisa Kit, Mercodia), triglyceride (TG) (glycerol phosphate oxidase [GPO]-Trinder method, Sigma) and free fatty acid (acyl coenzyme A synthetase [ACS-ACOD] method, Wako Diagnostics, Richmond, Va.).

Example 24 Calcitonin Fibril Formation

1 and 2 mg/ml of salmon calcitonin was prepared in PBS and incubated at 37° C. for 80 hrs. The kinetics of calcitonin amyloid fibril formation was monitored by measuring turbidity at 400 nm at different time interval. As shown in FIG. 29 the rate of fibril formation is concentration dependent and almost completed after 44 h. The SCA-I, SCA-II and SCA-III were formed at 12, 22 and 28 h, respectively.

In vitro Release of Calcitonin from Supramolecular Calcitonin Assembly

The release of free calcitonin from the SCA was monitored in 2% mannitol in constant volume of 1 ml and by dialyzing trough dialysis membrane. The release was monitored by absorbance at 275 nm. As shown in FIG. 30 the release of calcitonin from SCA in constant 1 ml follows bell shaped curve like insulin. However, continuous release was observed under dialysis through membrane and again was similar to insulin release from SIA. The release of calcitonin from fully grown calcitonin fiber was very slow and could be considered negligible for further experiment. The calcitonin SCA was further used for the in vivo experiments for the treatment of osteoporosis in ovariectomized rat.

Model for Osteoporosis and Treatment Using Calcitonin

44 female Sprague-Dawley rats (Charles River Laboratory, Wilmington, Mass.), approximately 90 days of age with an average body weight of 230 g were grouped into four groups at the beginning of the study. All rats were anesthetized with an intraperitoneal injection of ketamine hydrochloride and xylazine at doses of 50 and 10 mg/kg body weight (BW), respectively. Bilateral ovariectomies were performed in three groups from a dorsal approach. All rats were housed individually at 25° C. with a 12 h light/12 h dark cycle. The food consumption of ovariectomized (OVX) rats was restricted to that of the control rats to minimize increase in the body weight associated with ovariectomy. All rats were treated for 8 weeks with vehicle or Human/salmon CT (Sigma) either intermittently by subcutaneous injection or continuously by Alzet osmotic minipumps (Model 2ML4; Alza Corp., Palo Alto, Calif.) containing 200 μl of either CT (4 μg/kg) or SCA (Supramolecular calcitonin assembly) (2 mg/ml) in 2% mannitol, designed to deliver the solutions at a constant rate of 2.5 μl/h for 28 days. The intermittent treatments started a day after surgery. The minipumps for continuous CT or Calcitonin SCA or vehicle treatments were implanted at the time of surgery (day 0) and replaced after 3 weeks in case of continuous CT and vehicle treatment. However SCA injected during this period formed a depot which keeps on releasing calcitonin for up to about 6-8 weeks. For subcutaneous injections of CT, the hormone was dissolved in a vehicle of 2% mannitol. A dose of 16 IU/kg (4 μg/kg) body weight was chosen based on positive results from previous studies in OVX rats.

Half of the OVX rats from this group were injected subcutaneously on alternate days with 2% mannitol as a vehicle. The remaining OVX rats in this group were implanted subcutaneously with Alzet osmotic minipumps for continuous infusion of vehicle. Because statistically significant differences in bone variables were not observed between OVX rats treated with vehicle intermittently or continuously, the data from these subgroups have been combined.

Each OVX rat of one group was injected subcutaneously on alternate days with salmon CT at a dose of 16 U/kg BW (4 μg/kg b wt), and the other was implanted subcutaneously with an Alzet osmotic minipump for continuous infusion of human CT. The daily dose delivered to each rat by the minipump was 8 U/kg BW (2 μg/kg BW), which was equivalent to the dose given to the preceding group through subcutaneous injections on alternate days (16 U/kg).

Serum samples were stored at −80° C. until analyzed for their CT concentration by immunoassay methods with a commercially available kit (Bio-Merica). This kit was used to successfully measure serum salmon CT in rats in one of our previous studies. 15 Serum samples were also analyzed spectrophotometrically for their calcium and phosphorus contents by the cresolphthalein complexone and ammonium molybdate colorimetric methods, respectively (Table 3). FIG. 31 shows profile of calcitonin released from SCA-II in the serum of ovariectomized rat of different treatment group. Calcitonin in serum was measured by an immunoassay kit.

The antibody generated against salmon calcitonin in all the treated groups was monitored by indirect ELISA using monoclonal antibody for calcitonin. Data are expressed as the mean±standard deviation (SD) for each group. Statistical differences were evaluated by analysis of variance. P values<0.05 were considered to be significant.

Example 25 Covalent Conjugation of Peptide with Ibuprofen Using EDC

Dissolve the TTR/GNNQQNY to be modified at a concentration of 10 mg/ml in 0.1 MES, pH 4.7-6.0 containing NaCl (0.15 M). Dissolve the Ibuprofen to be coupled in the same buffer or added directly to the protein solution in the appropriate excess. Then added EDC to the above solution to obtain at least a 10 fold molar excess of EDC. Reacted for 2-3 hours at room temperature. Purified the conjugate by gel filtration or dialysis using buffer of choice (0.01M sodium phosphate, 0.15 M NaCl, pH 7.4).

Effect of Supramolecular Ibuprofen Assembly for Arthritis

Male wistar rats, weighing 180-220 g were selected and fed ad libitum. After four days of acclimatization, the rats were divided into five groups. Group I—control, Group II—Ibuprofen (10 mg/kg b.wt.), Group III—Ibuprofen (50 mg/kg b.wt.), Group IV—Ibuprofen coupled to transthyretin (TTR) or GNNQQNY injected intraperitoneally and Group V—carrageenin control. Groups II-V was anesthetized with halothane and KC arthritis was induced by an intra-articular injection of a mixture of 3% kaolin and 3% carrageenan (0.1 ml in sterile saline) into the synovial cavity of right knee joint. The joint was then manipulated by rapid flexion and extension movements for 1 min. Half an hour after injection of kaolin/carrageenan, the animals were treated as indicated above, with group II and II receiving daily injections of Ibuprofen orally. In the hot plate test method, rats from each group were placed on an analgesiometer, at a temperature of 55° C., and the latency in licking their paw was determined with a stop watch, one hour after treatment on day one (FIG. 32 a), and thereafter everyday for four days (FIG. 32 b). A 90-s cut-off time was imposed to prevent tissue damage.

Measurement of Paw Oedema

The paw volume was measured immediately before the injection of Kaolin/carrageenin and at hourly intervals thereafter for four days using a hydroplethysmometer (model 7150, Ugo Basile, Italy). The results were expressed as the increase in paw volume (ml) calculated by subtracting the basal volume (FIG. 33).

TABLE 1 Analysis of clinical parameters for the evaluation of toxicity of Supramolecular Insulin Assembly II (SIA II) Single daily Insulin Twice daily Parameters estimated Normal rats SIA II treated Injection Insulin Injection LFT Bilirubin (Total) (mg/dL) 0.35 ± 0.03 0.35 ± 0.06  0.40 ± 0.08* 0.35 ± 0.1 Bilirubin (Direct) (mg/dL) 0.108 ± 0.02   0.1 ± 0.03  0.36 ± 0.08* 0.25 ± 0.06* SGOT (U/L) 222.8 ± 79   219.8 ± 61     355 ± 83*  300 ± 56* SGPT (U/L) 74.8 ± 17   77 ± 21   86 ± 36   85 ± 15 Alkaline Phosphatase (U/L) 343.2 ± 76.8   431 ± 70.3 777.8 ± 89.4*  489 ± 65 Serum total proteins (g/dL)  3.92 ± 0.095 6.14 ± 0.3   6.70 ± 0.21* 5.55 ± 0.25* Serum Albumin (g/dL) 1.77 ± 0.11 1.85 ± 0.13  2.5 ± 0.21  3.2 ± 0.19 Serum Globulin (g/dL) 2.15 ± 0.08 2.64 ± 0.12  4.2 ± 0.18 3.35 ± 0.15 Serum A/G ratio 0.823 1.3 0.595 0.955 KFT Urea (mg/dL) 47.68 ± 10.8  50.9 ± 7.6   58.3 ± 9.2 60.1 ± 12.36 Serum Creatinine (mg/dL) 0.80 ± 0.06 0.83 ± 0.02  1.01 ± 0.30 0.88 ± 0.21 Uric Acid 2.39 ± 0.12 2.26 ± 0.08  3.0 ± 0.81  3.1 ± 0.56 Electrolytes Sodium (mEq/L) 140.6 ± 11   144 ± 10    200 ± 26  198 ± 45.5 Phosphorous (mEq/L)  4.5 ± 1.01 4.4 ± 1.1  6.5 ± 1.3  6.2 ± 0.95 Chloride (mEq/L) 102.8 ± 12   101 ± 17    165 ± 23  119 ± 26 Cataract Formation (−) (−) (+) (+) Adipose Tissue Normal Normal Decreased Decreased Body Weight and Appearance (+++) (+++) (+) (++)

TABLE 2 Effects of Treatments on the metabolic parameters of blood in fat-fed/streptozotocin-diabetic rats 1 week 2 week Rat Rat BGL Insulin FFA TG BGL Insulin FFA TG Group (mg/dL) (μU/ml) (mmol/L) (mmol/L) B W (mg/dL) (μU/ml) (mmol/L) (mmol/L) B W Control 107  20.5 ± 1.95 0.87 ± 0.10 0.48 ± 0.17 253 98 19.5 ± 1.5 0.89 ± 0.10 0.49 ± 0.17 260 Fat fed/STZ 477 39.48 ± 6.72 2.45 ± 0.07 0.86 ± 0.04 265 480  35.38 ± 10.18 2.55 ± 0.07 0.89 ± 0.04 271 Control Fat fed/STZ + 420 37.09 ± 4.7   1.9 ± 0.08 0.77 ± 0.05 261 401 37.09 ± 4.7   2.1 ± 0.08 0.75 ± 0.05 263 Insulin Fat fed/STZ + 180 34.83 ± 5.96  1.1 ± 0.06 0.68 ± 0.12 264 158 36.96 ± 5.04  1.0 ± 0.06 0.68 ± 0.12 268 Insulin SIA Fat fed/STZ + 157 31.58 ± 6.75 0.91 ± 0.11 0.51 ± 0.13 252 121 21.58 ± 6.75 0.88 ± 0.11 0.50 ± 0.13 259 Exendin-4 SA + insulin SIA 3 week 4 week Rat Rat BGL Insulin FFA TG BGL Insulin FFA TG Group (mg/dL) (μU/ml) (mmol/L) (mmol/L) B W (mg/dL) (μU/ml)) (mmol/L) (mmol/L) Control 100  20.1 ± 0.95 0.86 ± 0.10 0.51 ± 0.17 265 98  20.5 ± 1.95 0.9 ± 0.10 0.47 ± 0.17 Fat fed/STZ 506 39.55 ± 6.3  2.56 ± 0.07 0.91 ± 0.04 256 511 40.15 ± 1.35 2.59 ± 0.07 0.94 ± 0.04 Control Fat fed/STZ + 390 37.09 ± 4.7   1.8 ± 0.08 0.73 ± 0.05 269 396 37.09 ± 4.7  2.1 ± 0.08 0.76 ± 0.05 Insulin Fat fed/STZ + 149 36.96 ± 5.04  0.9 ± 0.06 0.68 ± 0.12 272 163 22.42 ± 8.70 1.1 ± 0.06 0.68 ± 0.12 Insulin SIA Fat fed/STZ + 119 19.40 ± 4.86 0.87 ± 0.11 0.48 ± 0.13 265 158 23.40 ± 4.86 0.98 ± 0.11 0.65 ± 0.13 Exendin-4 SA + insulin SIA

TABLE 3 Body weight and serum calcitonin, calcium, and phosphorus Groups Body Wt. Calcitonin Calcium Phosphorus Cont + VEH 296 ± 09 14.6 ± 2.9 10.0 ± 0.1  6.7 ± 0.6 OVX + VEH 328 ± 19 13.3 ± 2.1 11.2 ± 0.4  8.5 ± 1.1 OVX + CT 274 ± 10 15.3 ± 4.6 10.3 ± 0.4  7.6 ± 0.8 OVX + CT (MP) 280 ± 11 18.7 ± 5.0 9.5 ± 0.4 6.1 ± 0.7 OVX + SCA (MP) 276 ± 0.9 19.1 ± 4.2 9.3 ± 0.3 6.0 ± 0.6 Data are expressed as mean ± SD. p < 0.05 OVX + SCA vs. OVX + VEH; 

1-15. (canceled)
 16. A supramolecular calcitonin assembly (SCA) useful as protein therapeutics for the treatment of osteoporosis, wherein said assembly comprises insoluble and aggregated oligomeric form of calcitonin. 17-36. (canceled)
 37. A pharmaceutical composition for the treatment of osteoporosis, said composition comprising supramolecular calcitonin assembly (SCA) as claimed in claim
 16. 38. (canceled)
 39. The pharmaceutical composition as claimed in claim 37, wherein said composition upon administration releases calcitonin for about 55 to 60 days, wherein concentration of calcitonin released is in the range of 15-20 pg/ml. 40-44. (canceled)
 45. The pharmaceutical composition as claimed in claim 16 optionally comprises pharmaceutically acceptable carriers, additives or diluents.
 46. The pharmaceutical composition as claimed in claim 16 is administered intramuscularly, orally or subcutaneously, and/or wherein the pharmaceutical composition is administered through a device capable of releasing said composition, wherein said device is selected from a group consisting of pumps, catheters and implants. 47-51. (canceled)
 52. A process of preparation of supramolecular calcitonin assembly (SCA) as claimed in claim 16, said process comprising; a. dissolving calcitonin at a temperature of about 25 to 60° C., preferably 37° C., in a solution having pH in the range of about 4.0 to 8.0, preferably 6.8 to 7.4, most preferably 7.2; and b. incubating the above for a period of 6 to 48 hours preferably 8 to 12 hours, most preferably 8 hours with constant stirring to obtain Supramolecular Calcitonin Assembly (SCA), wherein SCA comprises insoluble and aggregated oligomeric form of calcitonin.
 53. The process as claimed in claim 52, wherein said process further comprises c. washing said SCA with PBS; and d. re-suspending said SCA in water or 2% mannitol. 54-73. (canceled)
 74. The pharmaceutical composition as claimed in claim 37 optionally comprises pharmaceutically acceptable carriers, additives or diluents.
 75. The pharmaceutical composition as claimed in claim 37 is administered intramuscularly, orally or subcutaneously, and/or wherein the pharmaceutical composition is administered through a device capable of releasing said composition, wherein said device is selected from a group consisting of pumps, catheters and implants.
 76. The pharmaceutical composition as claimed in claim 39 is administered intramuscularly, orally or subcutaneously, and/or wherein the pharmaceutical composition is administered through a device capable of releasing said composition, wherein said device is selected from a group consisting of pumps, catheters and implants.
 77. The pharmaceutical composition as claimed in claim 45 is administered intramuscularly, orally or subcutaneously, and/or wherein the pharmaceutical composition is administered through a device capable of releasing said composition, wherein said device is selected from a group consisting of pumps, catheters and implants. 